Rh > RHCE*03.26 RHCE*cE.26
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.48G>C p.Trp16Cys Exon 1 chr1:25,747,230 chr1:25,420,739
 
c.307C>T p.Pro103Ser Exon 2 chr1:25,735,202 chr1:25,408,711
 
 
 
 
 
 
 
 
Sequence
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