Canonical Allele Identifier: CA585155598
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1467640879

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601317_129601319del , CM000670.2:g.129601317_129601319del GRCh38
NC_000008.10:g.130613563_130613565del , CM000670.1:g.130613563_130613565del GRCh37
NC_000008.9:g.130682745_130682747del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78611_312+78613del