Canonical Allele Identifier: CA1819414151
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601273T= , CM000670.2:g.129601273T= GRCh38
NC_000008.10:g.130613519T= , CM000670.1:g.130613519T= GRCh37
NC_000008.9:g.130682701T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78655A=