Canonical Allele Identifier: CA2493477152

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011353T= , CM000664.2:g.21011353T=	GRCh38
NC_000002.11:g.21234225T= , CM000664.1:g.21234225T=	GRCh37
NC_000002.10:g.21087730T=	NCBI36
NG_011793.1:g.37721A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673739.2:c.*4821A=	ENSP00000501110.2:n.*4821A=
ENST00000673739.1:c.5229A=	ENSP00000501110.1:n.5229A=
ENST00000233242.5:c.5515A= MANE Select	ENSP00000233242.1:p.Ile1839=
ENST00000616098.4:c.5515A=	ENSP00000477990.1:p.Ile1839=
NM_000384.2:c.5515A=	NP_000375.2:p.Ile1839=
XM_011532809.1:c.5515A=	XP_011531111.1:p.Ile1839=
NM_000384.3:c.5515A= MANE Select	NP_000375.3:p.Ile1839=