Canonical Allele Identifier: CA2493479057

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21015495C= , CM000664.2:g.21015495C=	GRCh38
NC_000002.11:g.21238367C= , CM000664.1:g.21238367C=	GRCh37
NC_000002.10:g.21091872C=	NCBI36
NG_011793.1:g.33579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*2689G=	ENSP00000501110.2:n.*2689G=
ENST00000673882.2:c.*2478G=	ENSP00000501253.2:n.*2478G=
ENST00000673739.1:c.3097G=	ENSP00000501110.1:n.3097G=
ENST00000673882.1:c.2886G=	ENSP00000501253.1:n.2886G=
ENST00000233242.5:c.3383G= MANE Select	ENSP00000233242.1:p.Arg1128=
ENST00000616098.4:c.3383G=	ENSP00000477990.1:p.Arg1128=
NM_000384.2:c.3383G=	NP_000375.2:p.Arg1128=
XM_011532809.1:c.3383G=	XP_011531111.1:p.Arg1128=
NM_000384.3:c.3383G= MANE Select	NP_000375.3:p.Arg1128=