Canonical Allele Identifier: CA1819414237
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030290459

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601473A>C , CM000670.2:g.129601473A>C GRCh38
NC_000008.10:g.130613719A>C , CM000670.1:g.130613719A>C GRCh37
NC_000008.9:g.130682901A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.312+78455T>G