Canonical Allele Identifier: CA2187825630

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74751943T= , CM000677.2:g.74751943T=	GRCh38
NC_000015.9:g.75044284T= , CM000677.1:g.75044284T=	GRCh37
NC_000015.8:g.72831337T=	NCBI36
NG_008431.1:g.34402T=
NG_008431.2:g.34402T=
NG_061543.1:g.8099T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1042+89T= MANE Select	ENSP00000342007.4:n.1042+89T=
ENST00000343932.4:c.1042+89T=	ENSP00000342007.4:n.1042+89T=
NM_000761.4:c.1042+89T=	NP_000752.2:n.1042+89T=
NM_000761.5:c.1042+89T= MANE Select	NP_000752.2:n.1042+89T=