Canonical Allele Identifier: CA847373334
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1412202097

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465571T>A , CM000670.2:g.129465571T>A GRCh38
NC_000008.10:g.130477817T>A , CM000670.1:g.130477817T>A GRCh37
NC_000008.9:g.130546999T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15072A>T
NR_130918.1:n.138-95194A>T
NR_130919.1:n.138-65887A>T
NR_130920.1:n.138-65887A>T