Canonical Allele Identifier: CA2493479045

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015462G= , CM000664.2:g.21015462G=	GRCh38
NC_000002.11:g.21238334G= , CM000664.1:g.21238334G=	GRCh37
NC_000002.10:g.21091839G=	NCBI36
NG_011793.1:g.33612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2722C=	ENSP00000501110.2:n.*2722C=
ENST00000673882.2:c.*2511C=	ENSP00000501253.2:n.*2511C=
ENST00000673739.1:c.3130C=	ENSP00000501110.1:n.3130C=
ENST00000673882.1:c.2919C=	ENSP00000501253.1:n.2919C=
ENST00000233242.5:c.3416C= MANE Select	ENSP00000233242.1:p.Ala1139=
ENST00000616098.4:c.3416C=	ENSP00000477990.1:p.Ala1139=
NM_000384.2:c.3416C=	NP_000375.2:p.Ala1139=
XM_011532809.1:c.3416C=	XP_011531111.1:p.Ala1139=
NM_000384.3:c.3416C= MANE Select	NP_000375.3:p.Ala1139=