Canonical Allele Identifier: CA1819414302
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601605C= , CM000670.2:g.129601605C= GRCh38
NC_000008.10:g.130613851C= , CM000670.1:g.130613851C= GRCh37
NC_000008.9:g.130683033C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78323G=