Canonical Allele Identifier: CA12776126
Gene: CCDC26 HGNC NCBI

Linked Data

ClinVar Variation Id: 1711743
ClinVar RCV Id: RCV002293290
dbSNP Id: rs55705857
gnomAD v2: 8-130645692-A-G
gnomAD v3: 8-129633446-A-G
gnomAD v4: 8-129633446-A-G
MyVariant Identifiers: chr8:g.130645692A>G (hg19) chr8:g.129633446A>G (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633446A>G , CM000670.2:g.129633446A>G GRCh38
NC_000008.10:g.130645692A>G , CM000670.1:g.130645692A>G GRCh37
NC_000008.9:g.130714874A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46482T>C
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