ABO > ABO*AM.01
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.467C>T | p.Pro156Leu | Exon 7 | chr9:136,131,651 | chr9:133,256,235 |
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c.761C>T | p.Ala254Val | Exon 7 | chr9:136,131,357 | chr9:133,255,941 |
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Sequence
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