Yes. However, when we design assays for these applications, they are not competitive and so do not use two allele-specific forward primers and one common reverse primer like standard genotyping assay. Instead, we design one assay comprised of a (5’ tailed) forward primer and a reverse primer for the detection of one sequence and another assay of the same type for the detection of the other sequence. The two assays report with different fluorophores (FAM and HEX).