Canonical Allele Identifier: CA2658056067
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21011031-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011033dup , CM000664.2:g.21011033dup GRCh38
NC_000002.11:g.21233905dup , CM000664.1:g.21233905dup GRCh37
NC_000002.10:g.21087410dup NCBI36
NG_011793.1:g.38042dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5836dup MANE Select ENSP00000233242.1:p.Tyr1946LeufsTer12
ENST00000616098.4:c.5836dup ENSP00000477990.1:p.Tyr1946LeufsTer12
NM_000384.2:c.5836dup NP_000375.2:p.Tyr1946LeufsTer12
XM_011532809.1:c.5836dup XP_011531111.1:p.Tyr1946LeufsTer?
NM_000384.3:c.5836dup MANE Select NP_000375.3:p.Tyr1946LeufsTer12
Search 100 bp 5'
Search 100 bp 3'