Canonical Allele Identifier: CA2493492158

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21043836T= , CM000664.2:g.21043836T=	GRCh38
NC_000002.11:g.21266708T= , CM000664.1:g.21266708T=	GRCh37
NC_000002.10:g.21120213T=	NCBI36
NG_011793.1:g.5238A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.82+28A=	ENSP00000501110.2:n.82+28A=
ENST00000673882.2:c.82+28A=	ENSP00000501253.2:n.82+28A=
ENST00000233242.5:c.82+28A= MANE Select	ENSP00000233242.1:n.82+28A=
ENST00000399256.4:c.82+28A=	ENSP00000382200.4:n.82+28A=
ENST00000616098.4:c.82+28A=	ENSP00000477990.1:n.82+28A=
NM_000384.2:c.82+28A=	NP_000375.2:n.82+28A=
XM_011532809.1:c.82+28A=	XP_011531111.1:n.82+28A=
NM_000384.3:c.82+28A= MANE Select	NP_000375.3:n.82+28A=