Canonical Allele Identifier: CA2493489442

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038301T= , CM000664.2:g.21038301T=	GRCh38
NC_000002.11:g.21261173T= , CM000664.1:g.21261173T=	GRCh37
NC_000002.10:g.21114678T=	NCBI36
NG_011793.1:g.10773A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-1046A=	ENSP00000501110.2:n.384-1046A=
ENST00000673882.2:c.384-1046A=	ENSP00000501253.2:n.384-1046A=
ENST00000673739.1:c.252-1046A=	ENSP00000501110.1:n.252-1046A=
ENST00000673882.1:c.252-1046A=	ENSP00000501253.1:n.252-1046A=
ENST00000233242.5:c.384-190A= MANE Select	ENSP00000233242.1:n.384-190A=
ENST00000399256.4:c.384-190A=	ENSP00000382200.4:n.384-190A=
ENST00000616098.4:c.384-190A=	ENSP00000477990.1:n.384-190A=
NM_000384.2:c.384-190A=	NP_000375.2:n.384-190A=
XM_011532809.1:c.384-190A=	XP_011531111.1:n.384-190A=
NM_000384.3:c.384-190A= MANE Select	NP_000375.3:n.384-190A=