Canonical Allele Identifier: CA2586968928
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21009636-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009640del , CM000664.2:g.21009640del GRCh38
NC_000002.11:g.21232512del , CM000664.1:g.21232512del GRCh37
NC_000002.10:g.21086017del NCBI36
NG_011793.1:g.39437del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7231del MANE Select ENSP00000233242.1:p.Thr2411HisfsTer13
ENST00000616098.4:c.7231del ENSP00000477990.1:p.Thr2411HisfsTer13
NM_000384.2:c.7231del NP_000375.2:p.Thr2411HisfsTer13
XM_011532809.1:c.5869+1096del XP_011531111.1:n.5869+1096del
NM_000384.3:c.7231del MANE Select NP_000375.3:p.Thr2411HisfsTer13
Search 100 bp 5'
Search 100 bp 3'