Canonical Allele Identifier: CA43504666
Gene: APOB HGNC NCBI

Linked Data

ClinVar Variation Id: 128424
dbSNP Id: rs386643884

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.21009931_21009932delinsCA , CM000664.2:g.21009931_21009932delinsCA GRCh38
NC_000002.11:g.21232803_21232804delinsCA , CM000664.1:g.21232803_21232804delinsCA GRCh37
NC_000002.10:g.21086308_21086309delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000233242.5:c.6936_6937delinsTG MANE Select ENSP00000233242.1:p.Ile2313Val
ENST00000616098.4:c.6936_6937delinsTG ENSP00000477990.1:p.Ile2313Val
XM_011532809.1:c.5869+801_5869+802delinsTG XP_011531111.1:n.5869+801_5869+802delinsT...
NM_000384.3:c.6936_6937delinsTG MANE Select NP_000375.3:p.Ile2313Val