Canonical Allele Identifier: CA2187827281

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755322G= , CM000677.2:g.74755322G=	GRCh38
NC_000015.9:g.75047663G= , CM000677.1:g.75047663G=	GRCh37
NC_000015.8:g.72834716G=	NCBI36
NG_008431.1:g.37781G=
NG_008431.2:g.37781G=
NG_061543.1:g.11478G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*234G= MANE Select	ENSP00000342007.4:n.*234G=
ENST00000343932.4:c.*234G=	ENSP00000342007.4:n.*234G=
NM_000761.4:c.*234G=	NP_000752.2:n.*234G=
NM_000761.5:c.*234G= MANE Select	NP_000752.2:n.*234G=