ABO > ABO*O.16
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Phenotypes
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B
A,B
A1
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.106G>T p.Val36Phe Exon 3 chr9:136,136,774 chr9:133,261,358
 
c.188G>A p.Arg63His Exon 4 chr9:136,135,240 chr9:133,259,824
 
Sequence
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