Canonical Allele Identifier: CA916488024

Gene: APOB

Linked Data

• dbSNP Id: rs1572783978

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21011001_21011004del , CM000664.2:g.21011001_21011004del	GRCh38
NC_000002.11:g.21233873_21233876del , CM000664.1:g.21233873_21233876del	GRCh37
NC_000002.10:g.21087378_21087381del	NCBI36
NG_011793.1:g.38071_38074del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5865_5868del MANE Select	ENSP00000233242.1:p.Ser1956GlyfsTer?
ENST00000616098.4:c.5865_5868del	ENSP00000477990.1:p.Ser1956GlyfsTer?
NM_000384.2:c.5865_5868del	NP_000375.2:p.Ser1956GlyfsTer?
XM_011532809.1:c.5864+1_5864+4del
NM_000384.3:c.5865_5868del MANE Select	NP_000375.3:p.Ser1956GlyfsTer?