Canonical Allele Identifier: CA1819414152
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601274A= , CM000670.2:g.129601274A= GRCh38
NC_000008.10:g.130613520A= , CM000670.1:g.130613520A= GRCh37
NC_000008.9:g.130682702A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78654T=