Canonical Allele Identifier: CA186000950
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs373893621

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601381C>A , CM000670.2:g.129601381C>A GRCh38
NC_000008.10:g.130613627C>A , CM000670.1:g.130613627C>A GRCh37
NC_000008.9:g.130682809C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78547G>T