Canonical Allele Identifier: CA585154786
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1356081154

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465525C>T , CM000670.2:g.129465525C>T GRCh38
NC_000008.10:g.130477771C>T , CM000670.1:g.130477771C>T GRCh37
NC_000008.9:g.130546953C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.360+15118G>A
NR_130918.1:n.138-95148G>A
NR_130919.1:n.138-65841G>A
NR_130920.1:n.138-65841G>A