Canonical Allele Identifier: CA1819397313
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821515664

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560011_129560012dup , CM000670.2:g.129560011_129560012dup GRCh38
NC_000008.10:g.130572257_130572258dup , CM000670.1:g.130572257_130572258dup GRCh37
NC_000008.9:g.130641439_130641440dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79322_313-79321dup
NR_130918.1:n.137+14870_137+14871dup
NR_130919.1:n.137+14870_137+14871dup
NR_130920.1:n.137+14870_137+14871dup