Canonical Allele Identifier: CA2493479027

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015420G= , CM000664.2:g.21015420G=	GRCh38
NC_000002.11:g.21238292G= , CM000664.1:g.21238292G=	GRCh37
NC_000002.10:g.21091797G=	NCBI36
NG_011793.1:g.33654C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2764C=	ENSP00000501110.2:n.*2764C=
ENST00000673882.2:c.*2553C=	ENSP00000501253.2:n.*2553C=
ENST00000673739.1:c.3172C=	ENSP00000501110.1:n.3172C=
ENST00000673882.1:c.2961C=	ENSP00000501253.1:n.2961C=
ENST00000233242.5:c.3458C= MANE Select	ENSP00000233242.1:p.Ser1153=
ENST00000616098.4:c.3458C=	ENSP00000477990.1:p.Ser1153=
NM_000384.2:c.3458C=	NP_000375.2:p.Ser1153=
XM_011532809.1:c.3458C=	XP_011531111.1:p.Ser1153=
NM_000384.3:c.3458C= MANE Select	NP_000375.3:p.Ser1153=