Article
IVS5-38del4 deletion in the RHD gene does not cause a DEL phenotype: relevance for RHD alleles including DFR-3. von Zabern I, Flegel WA. Transfusion, 2007. [Citation]
Annotations by Allele
- RHD*486+1A (IVS3+1A, DEL8): otherHaplotype
- RHD*486+1A (IVS3+1A, DEL8): Prevalence
- RHD*505C,509G,514T (DFR1, RHD*17.01): RH1
- RHD*505C,509G,514T (DFR1, RHD*17.01): Serology
- RHD*505C,509G,514T (DFR1, RHD*17.01): otherHaplotype
- RHD*505C,509G,514T (DFR1, RHD*17.01): Prevalence
- RHD*505C,509G,514T (DFR1, RHD*17.01): otherHaplotype
- RHD*505C,509G,514T,539C (DFR3, RHD*17.03): otherHaplotype
- RHD*505C,509G,514T,539C (DFR3, RHD*17.03): Prevalence
- RHD*505C,509G,514T,539C (DFR3, RHD*17.03): RH1
- RHD*505C,509G,514T,539C (DFR3, RHD*17.03): RH1
- RHD*505C,509G,514T,539C (DFR3, RHD*17.03): Serology
- RHD*802-38delTCTC (IVS5-41delCTCT, DEL35): RH1
- RHD*802-38delTCTC (IVS5-41delCTCT, DEL35): otherHaplotype
- RHD*802-38delTCTC (IVS5-41delCTCT, DEL35): Serology
- RHD*802-38delTCTC (IVS5-41delCTCT, DEL35): otherHaplotype
- RHD*802-38delTCTC (IVS5-41delCTCT, DEL35): otherHaplotype
- RHD*802-38delTCTC (IVS5-41delCTCT, DEL35): Prevalence
- RHD*D-CE(4)-D (DFR2, RHD*17.02): RH1
- RHD*D-CE(4)-D (DFR2, RHD*17.02): RH1
- RHD*D-CE(4)-D (DFR2, RHD*17.02): Serology
- RHD*D-CE(4)-D (DFR2, RHD*17.02): otherHaplotype
- RHD*D-CE(4)-D (DFR2, RHD*17.02): Prevalence