Canonical Allele Identifier: CA186004574
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs920303313

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633407A>G , CM000670.2:g.129633407A>G GRCh38
NC_000008.10:g.130645653A>G , CM000670.1:g.130645653A>G GRCh37
NC_000008.9:g.130714835A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46521T>C