ABO > ABO*A2.18
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.467C>T | p.Pro156Leu | Exon 7 | chr9:136,131,651 | chr9:133,256,235 |
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c.722G>A | p.Arg241Gln | Exon 7 | chr9:136,131,396 | chr9:133,255,980 |
Sequence
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