Canonical Allele Identifier: CA2187827351

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755386T= , CM000677.2:g.74755386T=	GRCh38
NC_000015.9:g.75047727T= , CM000677.1:g.75047727T=	GRCh37
NC_000015.8:g.72834780T=	NCBI36
NG_008431.1:g.37845T=
NG_008431.2:g.37845T=
NG_061543.1:g.11542T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*298T= MANE Select	ENSP00000342007.4:n.*298T=
ENST00000343932.4:c.*298T=	ENSP00000342007.4:n.*298T=
NM_000761.4:c.*298T=	NP_000752.2:n.*298T=
NM_000761.5:c.*298T= MANE Select	NP_000752.2:n.*298T=