Canonical Allele Identifier: CA2187825595

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74751871A= , CM000677.2:g.74751871A=	GRCh38
NC_000015.9:g.75044212A= , CM000677.1:g.75044212A=	GRCh37
NC_000015.8:g.72831265A=	NCBI36
NG_008431.1:g.34330A=
NG_008431.2:g.34330A=
NG_061543.1:g.8027A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1042+17A= MANE Select	ENSP00000342007.4:n.1042+17A=
ENST00000343932.4:c.1042+17A=	ENSP00000342007.4:n.1042+17A=
NM_000761.4:c.1042+17A=	NP_000752.2:n.1042+17A=
NM_000761.5:c.1042+17A= MANE Select	NP_000752.2:n.1042+17A=