Canonical Allele Identifier: CA185996185
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs939559189

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560118A>C , CM000670.2:g.129560118A>C GRCh38
NC_000008.10:g.130572364A>C , CM000670.1:g.130572364A>C GRCh37
NC_000008.9:g.130641546A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79428T>G
NR_130918.1:n.137+14764T>G
NR_130919.1:n.137+14764T>G
NR_130920.1:n.137+14764T>G