Canonical Allele Identifier: CA1119153680
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030944681

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633311_129633312insTTGTATTGT , CM000670.2:g.129633311_129633312insTTGTATTGT GRCh38
NC_000008.10:g.130645557_130645558insTTGTATTGT , CM000670.1:g.130645557_130645558insTTGTATTGT GRCh37
NC_000008.9:g.130714739_130714740insTTGTATTGT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46616_312+46617insACAATACAA