ABO > ABO*A2.04
Allele Information
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Phenotypes
A
B
A,B
A1
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.297A>G Exon 6 chr9:136,132,873 chr9:133,257,457
 
c.526C>G p.Arg176Gly Exon 7 chr9:136,131,592 chr9:133,256,176
 
c.657C>T Exon 7 chr9:136,131,461 chr9:133,256,045
 
c.703G>A p.Gly235Ser Exon 7 chr9:136,131,415 chr9:133,255,999
 
c.771C>T Exon 7 chr9:136,131,347 chr9:133,255,931
 
c.829G>A p.Val277Met Exon 7 chr9:136,131,289 chr9:133,255,873
 
Sequence
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