Canonical Allele Identifier: CA2187827289

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755341A= , CM000677.2:g.74755341A=	GRCh38
NC_000015.9:g.75047682A= , CM000677.1:g.75047682A=	GRCh37
NC_000015.8:g.72834735A=	NCBI36
NG_008431.1:g.37800A=
NG_008431.2:g.37800A=
NG_061543.1:g.11497A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*253A= MANE Select	ENSP00000342007.4:n.*253A=
ENST00000343932.4:c.*253A=	ENSP00000342007.4:n.*253A=
NM_000761.4:c.*253A=	NP_000752.2:n.*253A=
NM_000761.5:c.*253A= MANE Select	NP_000752.2:n.*253A=