Canonical Allele Identifier: CA1819331942
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465553A= , CM000670.2:g.129465553A= GRCh38
NC_000008.10:g.130477799A= , CM000670.1:g.130477799A= GRCh37
NC_000008.9:g.130546981A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15090T=
NR_130918.1:n.138-95176T=
NR_130919.1:n.138-65869T=
NR_130920.1:n.138-65869T=