ABO > ABO*A2.11
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 |
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c.266C>T | p.Pro89Leu | Exon 6 | chr9:136,132,904 | chr9:133,257,488 |
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c.467C>T | p.Pro156Leu | Exon 7 | chr9:136,131,651 | chr9:133,256,235 |
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Sequence
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