ABO > ABO*O.02.04
Allele Information
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Phenotypes
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A,B
A1
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.53G>T p.Arg18Leu Exon 2 chr9:136,137,553 chr9:133,262,137
 
c.220C>T p.Pro74Ser Exon 5 chr9:136,133,508 chr9:133,258,092
 
c.297A>G Exon 6 chr9:136,132,873 chr9:133,257,457
 
c.488C>T p.Thr163Met Exon 7 chr9:136,131,630 chr9:133,256,214
 
c.526C>G p.Arg176Gly Exon 7 chr9:136,131,592 chr9:133,256,176
 
c.802G>A p.Gly268Arg Exon 7 chr9:136,131,316 chr9:133,255,900
 
Sequence
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