Canonical Allele Identifier: CA1119137304
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1820172109

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129465569A>G , CM000670.2:g.129465569A>G GRCh38
NC_000008.10:g.130477815A>G , CM000670.1:g.130477815A>G GRCh37
NC_000008.9:g.130546997A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.360+15074T>C
NR_130918.1:n.138-95192T>C
NR_130919.1:n.138-65885T>C
NR_130920.1:n.138-65885T>C