Canonical Allele Identifier: CA186004595
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1034913764

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633550A>C , CM000670.2:g.129633550A>C GRCh38
NC_000008.10:g.130645796A>C , CM000670.1:g.130645796A>C GRCh37
NC_000008.9:g.130714978A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+46378T>G