Canonical Allele Identifier: CA2576686516
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21007581del , CM000664.2:g.21007581del GRCh38
NC_000002.11:g.21230453del , CM000664.1:g.21230453del GRCh37
NC_000002.10:g.21083958del NCBI36
NG_011793.1:g.41493del

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.9287del MANE Select ENSP00000233242.1:p.Tyr3096LeufsTer20
ENST00000616098.4:c.9287del ENSP00000477990.1:p.Tyr3096LeufsTer20
NM_000384.2:c.9287del NP_000375.2:p.Tyr3096LeufsTer20
XM_011532809.1:c.5869+3152del XP_011531111.1:n.5869+3152del
NM_000384.3:c.9287del MANE Select NP_000375.3:p.Tyr3096LeufsTer20
Search 100 bp 5'
Search 100 bp 3'