Canonical Allele Identifier: CA1819397137

Gene: CCDC26

Linked Data

• dbSNP Id: rs1821512736

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.129559803G>A , CM000670.2:g.129559803G>A	GRCh38
NC_000008.10:g.130572049G>A , CM000670.1:g.130572049G>A	GRCh37
NC_000008.9:g.130641231G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_130917.1:n.313-79113C>T
NR_130918.1:n.137+15079C>T
NR_130919.1:n.137+15079C>T
NR_130920.1:n.137+15079C>T