Canonical Allele Identifier: CA1819414121
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601219T= , CM000670.2:g.129601219T= GRCh38
NC_000008.10:g.130613465T= , CM000670.1:g.130613465T= GRCh37
NC_000008.9:g.130682647T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78709A=