Canonical Allele Identifier: CA393169313
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754844A>T , CM000677.2:g.74754844A>T GRCh38
NC_000015.9:g.75047185A>T , CM000677.1:g.75047185A>T GRCh37
NC_000015.8:g.72834238A>T NCBI36
NG_008431.1:g.37303A>T
NG_008431.2:g.37303A>T
NG_061543.1:g.11000A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1307A>T MANE Select ENSP00000342007.4:p.Asp436Val
ENST00000343932.4:c.1307A>T ENSP00000342007.4:p.Asp436Val
NM_000761.4:c.1307A>T NP_000752.2:p.Asp436Val
NM_000761.5:c.1307A>T MANE Select NP_000752.2:p.Asp436Val