Canonical Allele Identifier: CA2493478949

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015238T= , CM000664.2:g.21015238T=	GRCh38
NC_000002.11:g.21238110T= , CM000664.1:g.21238110T=	GRCh37
NC_000002.10:g.21091615T=	NCBI36
NG_011793.1:g.33836A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2837A=	ENSP00000501110.2:n.*2837A=
ENST00000673882.2:c.*2626A=	ENSP00000501253.2:n.*2626A=
ENST00000673739.1:c.3245A=	ENSP00000501110.1:n.3245A=
ENST00000673882.1:c.3034A=	ENSP00000501253.1:n.3034A=
ENST00000233242.5:c.3531A= MANE Select	ENSP00000233242.1:p.Glu1177=
ENST00000616098.4:c.3531A=	ENSP00000477990.1:p.Glu1177=
NM_000384.2:c.3531A=	NP_000375.2:p.Glu1177=
XM_011532809.1:c.3531A=	XP_011531111.1:p.Glu1177=
NM_000384.3:c.3531A= MANE Select	NP_000375.3:p.Glu1177=