Canonical Allele Identifier: CA1819397430
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821517517

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560126A>C , CM000670.2:g.129560126A>C GRCh38
NC_000008.10:g.130572372A>C , CM000670.1:g.130572372A>C GRCh37
NC_000008.9:g.130641554A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79436T>G
NR_130918.1:n.137+14756T>G
NR_130919.1:n.137+14756T>G
NR_130920.1:n.137+14756T>G