Canonical Allele Identifier: CA2749094049
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009514del , CM000664.2:g.21009514del GRCh38
NC_000002.11:g.21232386del , CM000664.1:g.21232386del GRCh37
NC_000002.10:g.21085891del NCBI36
NG_011793.1:g.39561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7355del MANE Select ENSP00000233242.1:p.Gly2452ValfsTer15
ENST00000616098.4:c.7355del ENSP00000477990.1:p.Gly2452ValfsTer15
NM_000384.2:c.7355del NP_000375.2:p.Gly2452ValfsTer15
XM_011532809.1:c.5869+1220del XP_011531111.1:n.5869+1220del
NM_000384.3:c.7355del MANE Select NP_000375.3:p.Gly2452ValfsTer15
Search 100 bp 5'
Search 100 bp 3'