Canonical Allele Identifier: CA2187824390

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749316G= , CM000677.2:g.74749316G=	GRCh38
NC_000015.9:g.75041657G= , CM000677.1:g.75041657G=	GRCh37
NC_000015.8:g.72828710G=	NCBI36
NG_008431.1:g.31775G=
NG_008431.2:g.31775G=
NG_061543.1:g.5472G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.-9-414G= MANE Select	ENSP00000342007.4:n.-9-414G=
ENST00000343932.4:c.-9-414G=	ENSP00000342007.4:n.-9-414G=
NM_000761.4:c.-9-414G=	NP_000752.2:n.-9-414G=
NM_000761.5:c.-9-414G= MANE Select	NP_000752.2:n.-9-414G=