Canonical Allele Identifier: CA2187827306

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755357A= , CM000677.2:g.74755357A=	GRCh38
NC_000015.9:g.75047698A= , CM000677.1:g.75047698A=	GRCh37
NC_000015.8:g.72834751A=	NCBI36
NG_008431.1:g.37816A=
NG_008431.2:g.37816A=
NG_061543.1:g.11513A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*269A= MANE Select	ENSP00000342007.4:n.*269A=
ENST00000343932.4:c.*269A=	ENSP00000342007.4:n.*269A=
NM_000761.4:c.*269A=	NP_000752.2:n.*269A=
NM_000761.5:c.*269A= MANE Select	NP_000752.2:n.*269A=