Canonical Allele Identifier: CA2493473178

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21002881C= , CM000664.2:g.21002881C=	GRCh38
NC_000002.11:g.21225753C= , CM000664.1:g.21225753C=	GRCh37
NC_000002.10:g.21079258C=	NCBI36
NG_011793.1:g.46193G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.12541G= MANE Select	ENSP00000233242.1:p.Glu4181=
ENST00000616098.4:c.12541G=	ENSP00000477990.1:p.Glu4181=
NM_000384.2:c.12541G=	NP_000375.2:p.Glu4181=
XM_011532809.1:c.5870-3608G=	XP_011531111.1:n.5870-3608G=
NM_000384.3:c.12541G= MANE Select	NP_000375.3:p.Glu4181=