Canonical Allele Identifier: CA186004594
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1003887064

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633530G>A , CM000670.2:g.129633530G>A GRCh38
NC_000008.10:g.130645776G>A , CM000670.1:g.130645776G>A GRCh37
NC_000008.9:g.130714958G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46398C>T