Canonical Allele Identifier: CA1819427392
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030948430

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633525dup , CM000670.2:g.129633525dup GRCh38
NC_000008.10:g.130645771dup , CM000670.1:g.130645771dup GRCh37
NC_000008.9:g.130714953dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46403dup