Rh > RHCE*03.23 RHCE*cE.23
Allele Information
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.774T>A silent Exon 5 chr1:25,717,267 chr1:25,390,776
 
 
 
 
 
 
 
 
c.916A>G p.Ile306Val Exon 6 chr1:25,715,490 chr1:25,388,999
 
 
 
 
 
 
 
 
Sequence
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