Canonical Allele Identifier: CA1119160634
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821517923

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560165del , CM000670.2:g.129560165del GRCh38
NC_000008.10:g.130572411del , CM000670.1:g.130572411del GRCh37
NC_000008.9:g.130641593del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79475del
NR_130918.1:n.137+14717del
NR_130919.1:n.137+14717del
NR_130920.1:n.137+14717del