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Chromosome 19 - NC_000019.10
Genomic Sequence: NC_000019.10 Chromosome 19 Reference GRCh38.p14 Primary Assembly NC_060943.1 Chromosome 19 Alternate T2T-CHM13v2.0 NC_000019.9 Chromosome 19 Reference GRCh37.p13 Primary Assembly
Go to nucleotide: Graphics FASTA GenBank
Review eQTL and phenotype association data in this region using PheGenI
See variants in ClinVar
See studies and variants in dbVar
See Variation Viewer (GRCh37.p13)
See Variation Viewer (GRCh38)
NEW Try the new Transcript table
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.
NM_001366910.1 → NP_001353839.1 transmembrane protein 145 isoform 1 precursor
Status: VALIDATED
NM_173633.3 → NP_775904.2 transmembrane protein 145 isoform 2 precursor
See identical proteins and their annotated locations for NP_775904.2
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.
NC_000019.10 Reference GRCh38.p14 Primary Assembly
XM_011526791.4 → XP_011525093.1 transmembrane protein 145 isoform X1
XM_011526792.2 → XP_011525094.1 transmembrane protein 145 isoform X2
XM_047438636.1 → XP_047294592.1 transmembrane protein 145 isoform X3
NC_060943.1 Alternate T2T-CHM13v2.0
XM_054320623.1 → XP_054176598.1 transmembrane protein 145 isoform X1
XM_054320624.1 → XP_054176599.1 transmembrane protein 145 isoform X2
XM_054320625.1 → XP_054176600.1 transmembrane protein 145 isoform X3
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