Canonical Allele Identifier: CA1819331816
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820171148

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465497A>C , CM000670.2:g.129465497A>C GRCh38
NC_000008.10:g.130477743A>C , CM000670.1:g.130477743A>C GRCh37
NC_000008.9:g.130546925A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.360+15146T>G
NR_130918.1:n.138-95120T>G
NR_130919.1:n.138-65813T>G
NR_130920.1:n.138-65813T>G