Canonical Allele Identifier: CA2187827278

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755312T= , CM000677.2:g.74755312T=	GRCh38
NC_000015.9:g.75047653T= , CM000677.1:g.75047653T=	GRCh37
NC_000015.8:g.72834706T=	NCBI36
NG_008431.1:g.37771T=
NG_008431.2:g.37771T=
NG_061543.1:g.11468T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*224T= MANE Select	ENSP00000342007.4:n.*224T=
ENST00000343932.4:c.*224T=	ENSP00000342007.4:n.*224T=
NM_000761.4:c.*224T=	NP_000752.2:n.*224T=
NM_000761.5:c.*224T= MANE Select	NP_000752.2:n.*224T=