Canonical Allele Identifier: CA1819397131
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559801A= , CM000670.2:g.129559801A= GRCh38
NC_000008.10:g.130572047A= , CM000670.1:g.130572047A= GRCh37
NC_000008.9:g.130641229A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79111T=
NR_130918.1:n.137+15081T=
NR_130919.1:n.137+15081T=
NR_130920.1:n.137+15081T=