Canonical Allele Identifier: CA1119164160
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs2030287417

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129601292G>C , CM000670.2:g.129601292G>C GRCh38
NC_000008.10:g.130613538G>C , CM000670.1:g.130613538G>C GRCh37
NC_000008.9:g.130682720G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+78636C>G