Canonical Allele Identifier: CA2493489338

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038086C= , CM000664.2:g.21038086C=	GRCh38
NC_000002.11:g.21260958C= , CM000664.1:g.21260958C=	GRCh37
NC_000002.10:g.21114463C=	NCBI36
NG_011793.1:g.10988G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.384-831G=	ENSP00000501110.2:n.384-831G=
ENST00000673882.2:c.384-831G=	ENSP00000501253.2:n.384-831G=
ENST00000673739.1:c.252-831G=	ENSP00000501110.1:n.252-831G=
ENST00000673882.1:c.252-831G=	ENSP00000501253.1:n.252-831G=
ENST00000233242.5:c.409G= MANE Select	ENSP00000233242.1:p.Glu137=
ENST00000399256.4:c.409G=	ENSP00000382200.4:p.Glu137=
ENST00000616098.4:c.409G=	ENSP00000477990.1:p.Glu137=
NM_000384.2:c.409G=	NP_000375.2:p.Glu137=
XM_011532809.1:c.409G=	XP_011531111.1:p.Glu137=
NM_000384.3:c.409G= MANE Select	NP_000375.3:p.Glu137=