Canonical Allele Identifier: CA12776126
Gene: CCDC26 HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.129633446A>G
GRCh37 chr8:g.130645692A>G
gnomAD v2:
8:130645692 A / G
gnomAD v3:
8:129633446 A / G
gnomAD v4:
chr8-129633446-A-G
Joint Max Group AF 0.05470063 (NFE)
Genomes Max Group AF 0.05470063 (NFE)
ClinVar RCV:
RCV002293290
ClinVar Variation:
1711743
dbSNP:
55705857
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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
Search 100 bp 5'
Search 100 bp 3'