Canonical Allele Identifier: CA2604697365
Gene: CCDC26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633320A>G , CM000670.2:g.129633320A>G GRCh38
NC_000008.10:g.130645566A>G , CM000670.1:g.130645566A>G GRCh37
NC_000008.9:g.130714748A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46608T>C