Canonical Allele Identifier: CA2493472550

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21001649A= , CM000664.2:g.21001649A=	GRCh38
NC_000002.11:g.21224521A= , CM000664.1:g.21224521A=	GRCh37
NC_000002.10:g.21078026A=	NCBI36
NG_011793.1:g.47425T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.*81T= MANE Select	ENSP00000233242.1:n.*81T=
ENST00000616098.4:c.13771T=	ENSP00000477990.1:n.13771T=
NM_000384.2:c.*81T=	NP_000375.2:n.*81T=
XM_011532809.1:c.5870-2376T=	XP_011531111.1:n.5870-2376T=
NM_000384.3:c.*81T= MANE Select	NP_000375.3:n.*81T=