Canonical Allele Identifier: CA1119164155
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1275230737

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601281T>A , CM000670.2:g.129601281T>A GRCh38
NC_000008.10:g.130613527T>A , CM000670.1:g.130613527T>A GRCh37
NC_000008.9:g.130682709T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78647A>T