ABO > ABO*AW.42
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Phenotypes
A
B
A,B
A1
Genetic Changes
| nt change | aa change | Exon/Intron | HGVS | hg19 | hg38 | rsNum | gnomAD |
|---|---|---|---|---|---|---|---|
| c.467C>T | p.Pro156Leu | Exon 7 |
|
chr9:136,131,651 | chr9:133,256,235 |
|
|
| c.905A>G | p.Asp302Gly | Exon 7 |
|
chr9:136,131,213 | chr9:133,255,797 |
|
Sequence
None
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