Canonical Allele Identifier: CA1819468273
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129673211T>C , CM000670.2:g.129673211T>C GRCh38
NC_000008.10:g.130685457T>C , CM000670.1:g.130685457T>C GRCh37
NC_000008.9:g.130754639T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+6717A>G