Canonical Allele Identifier: CA916488032

Gene: APOB

Linked Data

• dbSNP Id: rs1572784004

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011012del , CM000664.2:g.21011012del	GRCh38
NC_000002.11:g.21233884del , CM000664.1:g.21233884del	GRCh37
NC_000002.10:g.21087389del	NCBI36
NG_011793.1:g.38062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5856del MANE Select	ENSP00000233242.1:p.His1953IlefsTer?
ENST00000616098.4:c.5856del	ENSP00000477990.1:p.His1953IlefsTer?
NM_000384.2:c.5856del	NP_000375.2:p.His1953IlefsTer?
XM_011532809.1:c.5856del	XP_011531111.1:p.His1953IlefsTer?
NM_000384.3:c.5856del MANE Select	NP_000375.3:p.His1953IlefsTer?