Canonical Allele Identifier: CA1819427407
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030948770

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633544A>G , CM000670.2:g.129633544A>G GRCh38
NC_000008.10:g.130645790A>G , CM000670.1:g.130645790A>G GRCh37
NC_000008.9:g.130714972A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46384T>C