Canonical Allele Identifier: CA2187827100

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754914C= , CM000677.2:g.74754914C=	GRCh38
NC_000015.9:g.75047255C= , CM000677.1:g.75047255C=	GRCh37
NC_000015.8:g.72834308C=	NCBI36
NG_008431.1:g.37373C=
NG_008431.2:g.37373C=
NG_061543.1:g.11070C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1377C= MANE Select	ENSP00000342007.4:p.Ile459=
ENST00000343932.4:c.1377C=	ENSP00000342007.4:p.Ile459=
NM_000761.4:c.1377C=	NP_000752.2:p.Ile459=
NM_000761.5:c.1377C= MANE Select	NP_000752.2:p.Ile459=