Canonical Allele Identifier: CA1819414285
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601565G= , CM000670.2:g.129601565G= GRCh38
NC_000008.10:g.130613811G= , CM000670.1:g.130613811G= GRCh37
NC_000008.9:g.130682993G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78363C=