Canonical Allele Identifier: CA645523823
Gene: APOB HGNC NCBI

Linked Data

COSMIC: COSM4612267
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007048del , CM000664.2:g.21007048del GRCh38
NC_000002.11:g.21229920del , CM000664.1:g.21229920del GRCh37
NC_000002.10:g.21083425del NCBI36
NG_011793.1:g.42027del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9821del MANE Select ENSP00000233242.1:p.Phe3274SerfsTer13
ENST00000616098.4:c.9821del ENSP00000477990.1:p.Phe3274SerfsTer13
NM_000384.2:c.9821del NP_000375.2:p.Phe3274SerfsTer13
XM_011532809.1:c.5869+3686del XP_011531111.1:n.5869+3686del
NM_000384.3:c.9821del MANE Select NP_000375.3:p.Phe3274SerfsTer13
Search 100 bp 5'
Search 100 bp 3'