Canonical Allele Identifier: CA1819331702
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465378T= , CM000670.2:g.129465378T= GRCh38
NC_000008.10:g.130477624T= , CM000670.1:g.130477624T= GRCh37
NC_000008.9:g.130546806T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15265A=
NR_130918.1:n.138-95001A=
NR_130919.1:n.138-65694A=
NR_130920.1:n.138-65694A=