Canonical Allele Identifier: CA2493479064

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015513C= , CM000664.2:g.21015513C=	GRCh38
NC_000002.11:g.21238385C= , CM000664.1:g.21238385C=	GRCh37
NC_000002.10:g.21091890C=	NCBI36
NG_011793.1:g.33561G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2671G=	ENSP00000501110.2:n.*2671G=
ENST00000673882.2:c.*2460G=	ENSP00000501253.2:n.*2460G=
ENST00000673739.1:c.3079G=	ENSP00000501110.1:n.3079G=
ENST00000673882.1:c.2868G=	ENSP00000501253.1:n.2868G=
ENST00000233242.5:c.3365G= MANE Select	ENSP00000233242.1:p.Gly1122=
ENST00000616098.4:c.3365G=	ENSP00000477990.1:p.Gly1122=
NM_000384.2:c.3365G=	NP_000375.2:p.Gly1122=
XM_011532809.1:c.3365G=	XP_011531111.1:p.Gly1122=
NM_000384.3:c.3365G= MANE Select	NP_000375.3:p.Gly1122=