Canonical Allele Identifier: CA1819414162
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030287280

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601288T>A , CM000670.2:g.129601288T>A GRCh38
NC_000008.10:g.130613534T>A , CM000670.1:g.130613534T>A GRCh37
NC_000008.9:g.130682716T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78640A>T