Canonical Allele Identifier: CA2586968927
Gene: APOB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009384_21009385insT , CM000664.2:g.21009384_21009385insT GRCh38
NC_000002.11:g.21232256_21232257insT , CM000664.1:g.21232256_21232257insT GRCh37
NC_000002.10:g.21085761_21085762insT NCBI36
NG_011793.1:g.39689_39690insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7483_7484insA MANE Select ENSP00000233242.1:p.Trp2495Ter
ENST00000616098.4:c.7483_7484insA ENSP00000477990.1:p.Trp2495Ter
NM_000384.2:c.7483_7484insA NP_000375.2:p.Trp2495Ter
XM_011532809.1:c.5869+1348_5869+1349insA XP_011531111.1:n.5869+1348_5869+1349insA
NM_000384.3:c.7483_7484insA MANE Select NP_000375.3:p.Trp2495Ter
Search 100 bp 5'
Search 100 bp 3'