Canonical Allele Identifier: CA186000948
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs10098310

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601368G>T , CM000670.2:g.129601368G>T GRCh38
NC_000008.10:g.130613614G>T , CM000670.1:g.130613614G>T GRCh37
NC_000008.9:g.130682796G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78560C>A