Canonical Allele Identifier: CA847392989
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1360294226

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601412A>C , CM000670.2:g.129601412A>C GRCh38
NC_000008.10:g.130613658A>C , CM000670.1:g.130613658A>C GRCh37
NC_000008.9:g.130682840A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78516T>G