Canonical Allele Identifier: CA1819427259
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030945402

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633363dup , CM000670.2:g.129633363dup GRCh38
NC_000008.10:g.130645609dup , CM000670.1:g.130645609dup GRCh37
NC_000008.9:g.130714791dup NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46569dup