Canonical Allele Identifier: CA1119164135
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030284357

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601219_129601220insACA , CM000670.2:g.129601219_129601220insACA GRCh38
NC_000008.10:g.130613465_130613466insACA , CM000670.1:g.130613465_130613466insACA GRCh37
NC_000008.9:g.130682647_130682648insACA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78708_312+78709insTGT