Canonical Allele Identifier: CA2493476471

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21009934C= , CM000664.2:g.21009934C=	GRCh38
NC_000002.11:g.21232806C= , CM000664.1:g.21232806C=	GRCh37
NC_000002.10:g.21086311C=	NCBI36
NG_011793.1:g.39140G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.6934G= MANE Select	ENSP00000233242.1:p.Asp2312=
ENST00000616098.4:c.6934G=	ENSP00000477990.1:p.Asp2312=
NM_000384.2:c.6934G=	NP_000375.2:p.Asp2312=
XM_011532809.1:c.5869+799G=	XP_011531111.1:n.5869+799G=
NM_000384.3:c.6934G= MANE Select	NP_000375.3:p.Asp2312=