Canonical Allele Identifier: CA2658056065

Gene: APOB

Linked Data

• gnomAD v4: 2-21010956-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.21010959del , CM000664.2:g.21010959del	GRCh38
NC_000002.11:g.21233831del , CM000664.1:g.21233831del	GRCh37
NC_000002.10:g.21087336del	NCBI36
NG_011793.1:g.38117del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233242.5:c.5911del MANE Select	ENSP00000233242.1:p.Leu1971CysfsTer?
ENST00000616098.4:c.5911del	ENSP00000477990.1:p.Leu1971CysfsTer?
NM_000384.2:c.5911del	NP_000375.2:p.Leu1971CysfsTer?
XM_011532809.1:c.5864+47del	XP_011531111.1:n.5864+47del
NM_000384.3:c.5911del MANE Select	NP_000375.3:p.Leu1971CysfsTer?