Canonical Allele Identifier: CA2493476971

Gene: APOB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011035C= , CM000664.2:g.21011035C=	GRCh38
NC_000002.11:g.21233907C= , CM000664.1:g.21233907C=	GRCh37
NC_000002.10:g.21087412C=	NCBI36
NG_011793.1:g.38039G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5833G= MANE Select	ENSP00000233242.1:p.Asp1945=
ENST00000616098.4:c.5833G=	ENSP00000477990.1:p.Asp1945=
NM_000384.2:c.5833G=	NP_000375.2:p.Asp1945=
XM_011532809.1:c.5833G=	XP_011531111.1:p.Asp1945=
NM_000384.3:c.5833G= MANE Select	NP_000375.3:p.Asp1945=