Canonical Allele Identifier: CA425345842
Gene: APOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.21233297_21233298insA (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21010425_21010426insA , CM000664.2:g.21010425_21010426insA GRCh38
NC_000002.11:g.21233297_21233298insA , CM000664.1:g.21233297_21233298insA GRCh37
NC_000002.10:g.21086802_21086803insA NCBI36
NG_011793.1:g.38648_38649insT

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6442_6443insT MANE Select ENSP00000233242.1:p.Lys2148IlefsTer3
ENST00000616098.4:c.6442_6443insT ENSP00000477990.1:p.Lys2148IlefsTer3
NM_000384.2:c.6442_6443insT NP_000375.2:p.Lys2148IlefsTer3
XM_011532809.1:c.5869+307_5869+308insT XP_011531111.1:n.5869+307_5869+308insT
NM_000384.3:c.6442_6443insT MANE Select NP_000375.3:p.Lys2148IlefsTer3
Search 100 bp 5'
Search 100 bp 3'