Canonical Allele Identifier: CA2493476476

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21009941T= , CM000664.2:g.21009941T=	GRCh38
NC_000002.11:g.21232813T= , CM000664.1:g.21232813T=	GRCh37
NC_000002.10:g.21086318T=	NCBI36
NG_011793.1:g.39133A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.6927A= MANE Select	ENSP00000233242.1:p.Arg2309=
ENST00000616098.4:c.6927A=	ENSP00000477990.1:p.Arg2309=
NM_000384.2:c.6927A=	NP_000375.2:p.Arg2309=
XM_011532809.1:c.5869+792A=	XP_011531111.1:n.5869+792A=
NM_000384.3:c.6927A= MANE Select	NP_000375.3:p.Arg2309=