Canonical Allele Identifier: CA1819414155
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601277T= , CM000670.2:g.129601277T= GRCh38
NC_000008.10:g.130613523T= , CM000670.1:g.130613523T= GRCh37
NC_000008.9:g.130682705T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78651A=