Canonical Allele Identifier: CA393170349
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754997T>A , CM000677.2:g.74754997T>A GRCh38
NC_000015.9:g.75047338T>A , CM000677.1:g.75047338T>A GRCh37
NC_000015.8:g.72834391T>A NCBI36
NG_008431.1:g.37456T>A
NG_008431.2:g.37456T>A
NG_061543.1:g.11153T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1460T>A MANE Select ENSP00000342007.4:p.Val487Glu
ENST00000343932.4:c.1460T>A ENSP00000342007.4:p.Val487Glu
NM_000761.4:c.1460T>A NP_000752.2:p.Val487Glu
NM_000761.5:c.1460T>A MANE Select NP_000752.2:p.Val487Glu