Canonical Allele Identifier: CA2187827096

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754907G= , CM000677.2:g.74754907G=	GRCh38
NC_000015.9:g.75047248G= , CM000677.1:g.75047248G=	GRCh37
NC_000015.8:g.72834301G=	NCBI36
NG_008431.1:g.37366G=
NG_008431.2:g.37366G=
NG_061543.1:g.11063G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1370G= MANE Select	ENSP00000342007.4:p.Arg457=
ENST00000343932.4:c.1370G=	ENSP00000342007.4:p.Arg457=
NM_000761.4:c.1370G=	NP_000752.2:p.Arg457=
NM_000761.5:c.1370G= MANE Select	NP_000752.2:p.Arg457=