Canonical Allele Identifier: CA2187827099

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754912A= , CM000677.2:g.74754912A=	GRCh38
NC_000015.9:g.75047253A= , CM000677.1:g.75047253A=	GRCh37
NC_000015.8:g.72834306A=	NCBI36
NG_008431.1:g.37371A=
NG_008431.2:g.37371A=
NG_061543.1:g.11068A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1375A= MANE Select	ENSP00000342007.4:p.Ile459=
ENST00000343932.4:c.1375A=	ENSP00000342007.4:p.Ile459=
NM_000761.4:c.1375A=	NP_000752.2:p.Ile459=
NM_000761.5:c.1375A= MANE Select	NP_000752.2:p.Ile459=