Canonical Allele Identifier: CA2658074510
Gene: APOB HGNC NCBI

Linked Data

gnomAD v4: 2-21005081-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21005084del , CM000664.2:g.21005084del GRCh38
NC_000002.11:g.21227956del , CM000664.1:g.21227956del GRCh37
NC_000002.10:g.21081461del NCBI36
NG_011793.1:g.43992del

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.11786del MANE Select ENSP00000233242.1:p.Asn3929MetfsTer13
ENST00000616098.4:c.11786del ENSP00000477990.1:p.Asn3929MetfsTer13
NM_000384.2:c.11786del NP_000375.2:p.Asn3929MetfsTer13
XM_011532809.1:c.5869+5651del XP_011531111.1:n.5869+5651del
NM_000384.3:c.11786del MANE Select NP_000375.3:p.Asn3929MetfsTer13
Search 100 bp 5'
Search 100 bp 3'