Canonical Allele Identifier: CA185985527
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1054980044

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465478T>C , CM000670.2:g.129465478T>C GRCh38
NC_000008.10:g.130477724T>C , CM000670.1:g.130477724T>C GRCh37
NC_000008.9:g.130546906T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.360+15165A>G
NR_130918.1:n.138-95101A>G
NR_130919.1:n.138-65794A>G
NR_130920.1:n.138-65794A>G