Canonical Allele Identifier: CA1819424160
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129629675A>T , CM000670.2:g.129629675A>T GRCh38
NC_000008.10:g.130641921A>T , CM000670.1:g.130641921A>T GRCh37
NC_000008.9:g.130711103A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+50253T>A