Canonical Allele Identifier: CA2493489293

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21038005G= , CM000664.2:g.21038005G=	GRCh38
NC_000002.11:g.21260877G= , CM000664.1:g.21260877G=	GRCh37
NC_000002.10:g.21114382G=	NCBI36
NG_011793.1:g.11069C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000673739.2:c.384-750C=	ENSP00000501110.2:n.384-750C=
ENST00000673882.2:c.384-750C=	ENSP00000501253.2:n.384-750C=
ENST00000673739.1:c.252-750C=	ENSP00000501110.1:n.252-750C=
ENST00000673882.1:c.252-750C=	ENSP00000501253.1:n.252-750C=
ENST00000233242.5:c.490C= MANE Select	ENSP00000233242.1:p.Leu164=
ENST00000399256.4:c.490C=	ENSP00000382200.4:p.Leu164=
ENST00000616098.4:c.490C=	ENSP00000477990.1:p.Leu164=
NM_000384.2:c.490C=	NP_000375.2:p.Leu164=
XM_011532809.1:c.490C=	XP_011531111.1:p.Leu164=
NM_000384.3:c.490C= MANE Select	NP_000375.3:p.Leu164=