Canonical Allele Identifier: CA1119153664
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030944317

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633305_129633306insTAAATACAATGTTGTTCATT , CM000670.2:g.129633305_129633306insTAAATACAATGTTGTTCATT GRCh38
NC_000008.10:g.130645551_130645552insTAAATACAATGTTGTTCATT , CM000670.1:g.130645551_130645552insTAAATACAATGTTGTTCATT GRCh37
NC_000008.9:g.130714733_130714734insTAAATACAATGTTGTTCATT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46622_312+46623insAATGAACAACATTGTATTTA