Canonical Allele Identifier: CA2493476926
Gene: APOB HGNC NCBI

Linked Data

dbSNP Id: rs1663298729
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010975dup , CM000664.2:g.21010975dup GRCh38
NC_000002.11:g.21233847dup , CM000664.1:g.21233847dup GRCh37
NC_000002.10:g.21087352dup NCBI36
NG_011793.1:g.38099dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000233242.5:c.5893dup MANE Select ENSP00000233242.1:p.Glu1965GlyfsTer12
ENST00000616098.4:c.5893dup ENSP00000477990.1:p.Glu1965GlyfsTer12
NM_000384.2:c.5893dup NP_000375.2:p.Glu1965GlyfsTer12
XM_011532809.1:c.5864+29dup XP_011531111.1:n.5864+29dup
NM_000384.3:c.5893dup MANE Select NP_000375.3:p.Glu1965GlyfsTer12
Search 100 bp 5'
Search 100 bp 3'