Canonical Allele Identifier: CA12776113
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs10956483

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559864G>C , CM000670.2:g.129559864G>C GRCh38
NC_000008.10:g.130572110G>C , CM000670.1:g.130572110G>C GRCh37
NC_000008.9:g.130641292G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.313-79174C>G
NR_130918.1:n.137+15018C>G
NR_130919.1:n.137+15018C>G
NR_130920.1:n.137+15018C>G