Canonical Allele Identifier: CA393179344
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1281521673

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750327G>A , CM000677.2:g.74750327G>A GRCh38
NC_000015.9:g.75042668G>A , CM000677.1:g.75042668G>A GRCh37
NC_000015.8:g.72829721G>A NCBI36
NG_008431.1:g.32786G>A
NG_008431.2:g.32786G>A
NG_061543.1:g.6483G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.589G>A MANE Select ENSP00000342007.4:p.Ala197Thr
ENST00000343932.4:c.589G>A ENSP00000342007.4:p.Ala197Thr
NM_000761.4:c.589G>A NP_000752.2:p.Ala197Thr
NM_000761.5:c.589G>A MANE Select NP_000752.2:p.Ala197Thr