Canonical Allele Identifier: CA7659801
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs774282507

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750264T>A , CM000677.2:g.74750264T>A GRCh38
NC_000015.9:g.75042605T>A , CM000677.1:g.75042605T>A GRCh37
NC_000015.8:g.72829658T>A NCBI36
NG_008431.1:g.32723T>A
NG_008431.2:g.32723T>A
NG_061543.1:g.6420T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.526T>A MANE Select ENSP00000342007.4:p.Leu176Met
ENST00000343932.4:c.526T>A ENSP00000342007.4:p.Leu176Met
NM_000761.4:c.526T>A NP_000752.2:p.Leu176Met
NM_000761.5:c.526T>A MANE Select NP_000752.2:p.Leu176Met