Canonical Allele Identifier: CA7660055
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs763121117

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754766C>A , CM000677.2:g.74754766C>A GRCh38
NC_000015.9:g.75047107C>A , CM000677.1:g.75047107C>A GRCh37
NC_000015.8:g.72834160C>A NCBI36
NG_008431.1:g.37225C>A
NG_008431.2:g.37225C>A
NG_061543.1:g.10922C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-25C>A MANE Select ENSP00000342007.4:n.1254-25C>A
ENST00000343932.4:c.1254-25C>A ENSP00000342007.4:n.1254-25C>A
NM_000761.4:c.1254-25C>A NP_000752.2:n.1254-25C>A
NM_000761.5:c.1254-25C>A MANE Select NP_000752.2:n.1254-25C>A