Canonical Allele Identifier: CA1119160584
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821516049

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560038G>A , CM000670.2:g.129560038G>A GRCh38
NC_000008.10:g.130572284G>A , CM000670.1:g.130572284G>A GRCh37
NC_000008.9:g.130641466G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79348C>T
NR_130918.1:n.137+14844C>T
NR_130919.1:n.137+14844C>T
NR_130920.1:n.137+14844C>T