Canonical Allele Identifier: CA2187827333

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755370C= , CM000677.2:g.74755370C=	GRCh38
NC_000015.9:g.75047711C= , CM000677.1:g.75047711C=	GRCh37
NC_000015.8:g.72834764C=	NCBI36
NG_008431.1:g.37829C=
NG_008431.2:g.37829C=
NG_061543.1:g.11526C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*282C= MANE Select	ENSP00000342007.4:n.*282C=
ENST00000343932.4:c.*282C=	ENSP00000342007.4:n.*282C=
NM_000761.4:c.*282C=	NP_000752.2:n.*282C=
NM_000761.5:c.*282C= MANE Select	NP_000752.2:n.*282C=