Canonical Allele Identifier: CA2493472869

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21002227T= , CM000664.2:g.21002227T=	GRCh38
NC_000002.11:g.21225099T= , CM000664.1:g.21225099T=	GRCh37
NC_000002.10:g.21078604T=	NCBI36
NG_011793.1:g.46847A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233242.5:c.13195A= MANE Select	ENSP00000233242.1:p.Lys4399=
ENST00000616098.4:c.13193A=	ENSP00000477990.1:n.13193A=
NM_000384.2:c.13195A=	NP_000375.2:p.Lys4399=
XM_011532809.1:c.5870-2954A=	XP_011531111.1:n.5870-2954A=
NM_000384.3:c.13195A= MANE Select	NP_000375.3:p.Lys4399=