A novel RHD allele caused by c.687_689delAAG variant.

The authors have disclosed no conflicts of interest. Figure S1. Sequence analysis of the partial exon 5 region of the RHD gene. The variant sequence and the corresponding wild-type sequence are shown in the bottom and top rows, respectively. The arrow indicates a novel c.687_689delAAG variant and the corresponding wild-type nucleotides are underlined. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.