Canonical Allele Identifier: CA847371650
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1201626008

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129559772A>G , CM000670.2:g.129559772A>G GRCh38
NC_000008.10:g.130572018A>G , CM000670.1:g.130572018A>G GRCh37
NC_000008.9:g.130641200A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79082T>C
NR_130918.1:n.137+15110T>C
NR_130919.1:n.137+15110T>C
NR_130920.1:n.137+15110T>C