Canonical Allele Identifier: CA913187930
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663245532
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009481_21009482delinsG , CM000664.2:g.21009481_21009482delinsG GRCh38
NC_000002.11:g.21232353_21232354delinsG , CM000664.1:g.21232353_21232354delinsG GRCh37
NC_000002.10:g.21085858_21085859delinsG NCBI36
NG_011793.1:g.39592_39593delinsC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.7386_7387delinsC MANE Select ENSP00000233242.1:p.Lys2462AsnfsTer5
ENST00000616098.4:c.7386_7387delinsC ENSP00000477990.1:p.Lys2462AsnfsTer5
NM_000384.2:c.7386_7387delinsC NP_000375.2:p.Lys2462AsnfsTer5
XM_011532809.1:c.5869+1251_5869+1252delinsC XP_011531111.1:n.5869+1251_5869+1252delinsC
NM_000384.3:c.7386_7387delinsC MANE Select NP_000375.3:p.Lys2462AsnfsTer5
Search 100 bp 5'
Search 100 bp 3'