Canonical Allele Identifier: CA645523822
Gene: APOB HGNC NCBI

Linked Data

COSMIC: COSM5701688
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21006957_21006958delinsGC , CM000664.2:g.21006957_21006958delinsGC GRCh38
NC_000002.11:g.21229829_21229830delinsGC , CM000664.1:g.21229829_21229830delinsGC GRCh37
NC_000002.10:g.21083334_21083335delinsGC NCBI36
NG_011793.1:g.42116_42117delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.9910_9911delinsGC MANE Select ENSP00000233242.1:p.Leu3304Ala
ENST00000616098.4:c.9910_9911delinsGC ENSP00000477990.1:p.Leu3304Ala
NM_000384.2:c.9910_9911delinsGC NP_000375.2:p.Leu3304Ala
XM_011532809.1:c.5869+3775_5869+3776delinsGC XP_011531111.1:n.5869+3775_5869+3776delinsGC
NM_000384.3:c.9910_9911delinsGC MANE Select NP_000375.3:p.Leu3304Ala
Search 100 bp 5'
Search 100 bp 3'