Canonical Allele Identifier: CA1819414178
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030287820

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601314T>G , CM000670.2:g.129601314T>G GRCh38
NC_000008.10:g.130613560T>G , CM000670.1:g.130613560T>G GRCh37
NC_000008.9:g.130682742T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78614A>C