Canonical Allele Identifier: CA186004591
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs771890163

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633506C>T , CM000670.2:g.129633506C>T GRCh38
NC_000008.10:g.130645752C>T , CM000670.1:g.130645752C>T GRCh37
NC_000008.9:g.130714934C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46422G>A