These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

RNA

1. NR_146444.1 RNA Sequence

   Status: VALIDATED

   Description

   Transcript Variant: This variant (1) represents the longest transcript.

   Source sequence(s)

   AC008759

2. NR_146445.1 RNA Sequence

   Status: VALIDATED

   Description

   Transcript Variant: This variant (2) lacks an alternate exon compared to variant 1.

   Source sequence(s)

   AC008759

3. NR_146446.1 RNA Sequence

   Status: VALIDATED

   Description

   Transcript Variant: This variant (3) lacks two alternate exons compared to variant 1.

   Source sequence(s)

   AC008759

The following sections contain reference sequences that belong to a specific genome build. Explain

This section includes genomic Reference Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate assemblies. Model RNAs and proteins are also reported here.

Reference GRCh38.p14 Primary Assembly

Genomic

1. NC_000019.10 Reference GRCh38.p14 Primary Assembly

   Range

   9688860..9700776 complement

   Download

   GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

1. NC_060943.1 Alternate T2T-CHM13v2.0

   Range

   9815049..9826957 complement

   Download

   GenBank, FASTA, Sequence Viewer (Graphics)

The following Reference Sequences have been suppressed. Explain

These RefSeqs were suppressed for the cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related sequence links, or BLAST links (BLink), but may still be retrieved by clicking on their accession.version below.

1. NM_001199814.1: Suppressed sequence

   Description

   NM_001199814.1: This RefSeq was removed because it is now thought that this gene is a pseudogene.