Canonical Allele Identifier: CA393179116
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs756244484

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750250C>T , CM000677.2:g.74750250C>T GRCh38
NC_000015.9:g.75042591C>T , CM000677.1:g.75042591C>T GRCh37
NC_000015.8:g.72829644C>T NCBI36
NG_008431.1:g.32709C>T
NG_008431.2:g.32709C>T
NG_061543.1:g.6406C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.512C>T MANE Select ENSP00000342007.4:p.Ala171Val
ENST00000343932.4:c.512C>T ENSP00000342007.4:p.Ala171Val
NM_000761.4:c.512C>T NP_000752.2:p.Ala171Val
NM_000761.5:c.512C>T MANE Select NP_000752.2:p.Ala171Val