Canonical Allele Identifier: CA2187824831

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74750314G= , CM000677.2:g.74750314G=	GRCh38
NC_000015.9:g.75042655G= , CM000677.1:g.75042655G=	GRCh37
NC_000015.8:g.72829708G=	NCBI36
NG_008431.1:g.32773G=
NG_008431.2:g.32773G=
NG_061543.1:g.6470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.576G= MANE Select	ENSP00000342007.4:p.Val192=
ENST00000343932.4:c.576G=	ENSP00000342007.4:p.Val192=
NM_000761.4:c.576G=	NP_000752.2:p.Val192=
NM_000761.5:c.576G= MANE Select	NP_000752.2:p.Val192=