Canonical Allele Identifier: CA1119160563
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821515168

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559971G>A , CM000670.2:g.129559971G>A GRCh38
NC_000008.10:g.130572217G>A , CM000670.1:g.130572217G>A GRCh37
NC_000008.9:g.130641399G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79281C>T
NR_130918.1:n.137+14911C>T
NR_130919.1:n.137+14911C>T
NR_130920.1:n.137+14911C>T