Canonical Allele Identifier: CA2493484936

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21028395C= , CM000664.2:g.21028395C=	GRCh38
NC_000002.11:g.21251267C= , CM000664.1:g.21251267C=	GRCh37
NC_000002.10:g.21104772C=	NCBI36
NG_011793.1:g.20679G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.*1067G=	ENSP00000501110.2:n.*1067G=
ENST00000673882.2:c.*1067G=	ENSP00000501253.2:n.*1067G=
ENST00000673739.1:c.1475G=	ENSP00000501110.1:n.1475G=
ENST00000673882.1:c.1475G=	ENSP00000501253.1:n.1475G=
ENST00000233242.5:c.1761G= MANE Select	ENSP00000233242.1:p.Glu587=
ENST00000399256.4:c.1761G=	ENSP00000382200.4:p.Glu587=
ENST00000616098.4:c.1761G=	ENSP00000477990.1:p.Glu587=
NM_000384.2:c.1761G=	NP_000375.2:p.Glu587=
XM_011532809.1:c.1761G=	XP_011531111.1:p.Glu587=
NM_000384.3:c.1761G= MANE Select	NP_000375.3:p.Glu587=