All sequences should have a unique name (e.g. >Target Name 1) on a line separate from the sequence.
The SNP site should be specified as [reference/alternate] to indicate the alleles in this format [X/Y]. Enter only one target SNP per sequence.
Only biallelic SNPs are allowed unless using SNP Assay Beta design.
The SNP site should be specified as [reference/alternate] to indicate the two alleles in this format [X/Y]. Enter only one target SNP per sequence.
Only biallelic SNPs are allowed, indels, triallelic and tetra-allelic variants are not currently supported.
Sequence should follow IUPAC code for DNA bases (except SNP site of interest).
Mixed base codes should be avoided within 20 nt of the SNP site, as they will affect the ability to design an assay.