Canonical Allele Identifier: CA1819397378
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1821516576

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129560060T>G , CM000670.2:g.129560060T>G GRCh38
NC_000008.10:g.130572306T>G , CM000670.1:g.130572306T>G GRCh37
NC_000008.9:g.130641488T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_130917.1:n.313-79370A>C
NR_130918.1:n.137+14822A>C
NR_130919.1:n.137+14822A>C
NR_130920.1:n.137+14822A>C