ClinVar

NM_001256643.1(LTA4H):c.88-6908C>T

Gene:

LTA4H:leukotriene A4 hydrolase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q23.1

Genomic location:

• Chr12: 96036093 (on Assembly GRCh38)
• Chr12: 96429871 (on Assembly GRCh37)

Preferred name:

NM_001256643.1(LTA4H):c.88-6908C>T

HGVS:

• NC_000012.12:g.96036093G>A
• NM_001256643.1:c.88-6908C>T
• NM_001256644.1:c.88-6908C>T
• NC_000012.11:g.96429871G>A
• NT_029419.12:g.58573177G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs281860641

NCBI 1000 Genomes Browser:

rs281860641

Molecular consequence:

• NM_001256643.1:c.88-6908C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001256644.1:c.88-6908C>T - intron variant - [Sequence Ontology: SO:0001627]