Canonical Allele Identifier: CA1819397235
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559917A= , CM000670.2:g.129559917A= GRCh38
NC_000008.10:g.130572163A= , CM000670.1:g.130572163A= GRCh37
NC_000008.9:g.130641345A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79227T=
NR_130918.1:n.137+14965T=
NR_130919.1:n.137+14965T=
NR_130920.1:n.137+14965T=