Canonical Allele Identifier: CA2493478955

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015253C= , CM000664.2:g.21015253C=	GRCh38
NC_000002.11:g.21238125C= , CM000664.1:g.21238125C=	GRCh37
NC_000002.10:g.21091630C=	NCBI36
NG_011793.1:g.33821G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2822G=	ENSP00000501110.2:n.*2822G=
ENST00000673882.2:c.*2611G=	ENSP00000501253.2:n.*2611G=
ENST00000673739.1:c.3230G=	ENSP00000501110.1:n.3230G=
ENST00000673882.1:c.3019G=	ENSP00000501253.1:n.3019G=
ENST00000233242.5:c.3516G= MANE Select	ENSP00000233242.1:p.Glu1172=
ENST00000616098.4:c.3516G=	ENSP00000477990.1:p.Glu1172=
NM_000384.2:c.3516G=	NP_000375.2:p.Glu1172=
XM_011532809.1:c.3516G=	XP_011531111.1:p.Glu1172=
NM_000384.3:c.3516G= MANE Select	NP_000375.3:p.Glu1172=