Canonical Allele Identifier: CA2187825549

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74751799C= , CM000677.2:g.74751799C=	GRCh38
NC_000015.9:g.75044140C= , CM000677.1:g.75044140C=	GRCh37
NC_000015.8:g.72831193C=	NCBI36
NG_008431.1:g.34258C=
NG_008431.2:g.34258C=
NG_061543.1:g.7955C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.987C= MANE Select	ENSP00000342007.4:p.Ser329=
ENST00000343932.4:c.987C=	ENSP00000342007.4:p.Ser329=
NM_000761.4:c.987C=	NP_000752.2:p.Ser329=
NM_000761.5:c.987C= MANE Select	NP_000752.2:p.Ser329=