Canonical Allele Identifier: CA1819397398
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821516899

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560081_129560084dup , CM000670.2:g.129560081_129560084dup GRCh38
NC_000008.10:g.130572327_130572330dup , CM000670.1:g.130572327_130572330dup GRCh37
NC_000008.9:g.130641509_130641512dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79392_313-79389dup
NR_130918.1:n.137+14800_137+14803dup
NR_130919.1:n.137+14800_137+14803dup
NR_130920.1:n.137+14800_137+14803dup