Canonical Allele Identifier: CA1819414100
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601179T= , CM000670.2:g.129601179T= GRCh38
NC_000008.10:g.130613425T= , CM000670.1:g.130613425T= GRCh37
NC_000008.9:g.130682607T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78749A=