Canonical Allele Identifier: CA2187825589

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74751863G= , CM000677.2:g.74751863G=	GRCh38
NC_000015.9:g.75044204G= , CM000677.1:g.75044204G=	GRCh37
NC_000015.8:g.72831257G=	NCBI36
NG_008431.1:g.34322G=
NG_008431.2:g.34322G=
NG_061543.1:g.8019G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1042+9G= MANE Select	ENSP00000342007.4:n.1042+9G=
ENST00000343932.4:c.1042+9G=	ENSP00000342007.4:n.1042+9G=
NM_000761.4:c.1042+9G=	NP_000752.2:n.1042+9G=
NM_000761.5:c.1042+9G= MANE Select	NP_000752.2:n.1042+9G=