Canonical Allele Identifier: CA1819414208
Gene: CCDC26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601413A= , CM000670.2:g.129601413A= GRCh38
NC_000008.10:g.130613659A= , CM000670.1:g.130613659A= GRCh37
NC_000008.9:g.130682841A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78515T=