Canonical Allele Identifier: CA2493472812

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21002143C= , CM000664.2:g.21002143C=	GRCh38
NC_000002.11:g.21225015C= , CM000664.1:g.21225015C=	GRCh37
NC_000002.10:g.21078520C=	NCBI36
NG_011793.1:g.46931G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.13279G= MANE Select	ENSP00000233242.1:p.Val4427=
ENST00000616098.4:c.13277G=	ENSP00000477990.1:n.13277G=
NM_000384.2:c.13279G=	NP_000375.2:p.Val4427=
XM_011532809.1:c.5870-2870G=	XP_011531111.1:n.5870-2870G=
NM_000384.3:c.13279G= MANE Select	NP_000375.3:p.Val4427=