Canonical Allele Identifier: CA1819397469
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560180C= , CM000670.2:g.129560180C= GRCh38
NC_000008.10:g.130572426C= , CM000670.1:g.130572426C= GRCh37
NC_000008.9:g.130641608C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79490G=
NR_130918.1:n.137+14702G=
NR_130919.1:n.137+14702G=
NR_130920.1:n.137+14702G=