Canonical Allele Identifier: CA2782190027
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559788G>T , CM000670.2:g.129559788G>T GRCh38
NC_000008.10:g.130572034G>T , CM000670.1:g.130572034G>T GRCh37
NC_000008.9:g.130641216G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79098C>A
NR_130918.1:n.137+15094C>A
NR_130919.1:n.137+15094C>A
NR_130920.1:n.137+15094C>A