Canonical Allele Identifier: CA12776126
Gene: CCDC26 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs55705857

User contributed link-outs

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