Canonical Allele Identifier: CA916488031
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1572783997
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21011009_21011010insC , CM000664.2:g.21011009_21011010insC GRCh38
NC_000002.11:g.21233881_21233882insC , CM000664.1:g.21233881_21233882insC GRCh37
NC_000002.10:g.21087386_21087387insC NCBI36
NG_011793.1:g.38064_38065insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5858_5859insG MANE Select ENSP00000233242.1:p.His1953GlnfsTer5
ENST00000616098.4:c.5858_5859insG ENSP00000477990.1:p.His1953GlnfsTer5
NM_000384.2:c.5858_5859insG NP_000375.2:p.His1953GlnfsTer5
XM_011532809.1:c.5858_5859insG XP_011531111.1:p.His1953GlnfsTer?
NM_000384.3:c.5858_5859insG MANE Select NP_000375.3:p.His1953GlnfsTer5
Search 100 bp 5'
Search 100 bp 3'