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The effects of transferring brown midrib (bmr) alleles in sweet and high biomass sorghums (SS/HBM) are not fully understood, and available works produced mixed results depending upon the genetic background of the recurrent parent used. Early-generation testing of the effects of the two mutations in the background of the recurrent parents can help predict the final products and make appropriate early go/no-go breeding decisions, yet, this information is missing. The present study was therefore carried out to reduce these gaps. Marker-assisted transfer of the bmr6 and bmr12 was performed using four (SSV84, ICSB474, ICSV18003, ICSV100324) SS and one (ICSV15024) HBM wild type (WT) lines as recurrent parents, and one bmr6 (N609) and two bmr12 (ICSV101039 and N600) lines as donor parents. Crossing and backcrossing techniques were used to transfer the bmr alleles to develop BC2F2 and F3 populations. Kompetitive allele-specific PCR (KASP) marker genotyping assays were performed and implemented for the indirect selection of the bmr transfer in F1 and BC_F1 populations. While the bmr6 markers were polymorphic, the bmr12 markers were monomorphic. The successful bmr6 transfer was therefore confirmed by markers in F1 and BC_F1, while for bmr12 the transfer was confirmed after segregation assessment in F2 and BC_F2 populations. The transfer of bmr12 improved the cellulose content relative to WT genotypes, and bmr12 populations were shorter-statured relative to bmr6 individuals, meaning that bmr12 gene can be considered in sorghum breeding to boost 2G bioethanol bioconversion and to control lodging, and …