Canonical Allele Identifier: CA1819331871
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465529C= , CM000670.2:g.129465529C= GRCh38
NC_000008.10:g.130477775C= , CM000670.1:g.130477775C= GRCh37
NC_000008.9:g.130546957C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15114G=
NR_130918.1:n.138-95152G=
NR_130919.1:n.138-65845G=
NR_130920.1:n.138-65845G=