Canonical Allele Identifier: CA2187824612

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749842T= , CM000677.2:g.74749842T=	GRCh38
NC_000015.9:g.75042183T= , CM000677.1:g.75042183T=	GRCh37
NC_000015.8:g.72829236T=	NCBI36
NG_008431.1:g.32301T=
NG_008431.2:g.32301T=
NG_061543.1:g.5998T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.104T= MANE Select	ENSP00000342007.4:p.Val35=
ENST00000343932.4:c.104T=	ENSP00000342007.4:p.Val35=
NM_000761.4:c.104T=	NP_000752.2:p.Val35=
NM_000761.5:c.104T= MANE Select	NP_000752.2:p.Val35=