ABO > ABO*AEL.07
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.681G>A | Exon 7 | chr9:136,131,437 | chr9:133,256,021 |
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c.771C>T | Exon 7 | chr9:136,131,347 | chr9:133,255,931 |
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c.829G>A | p.Val277Met | Exon 7 | chr9:136,131,289 | chr9:133,255,873 |
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Sequence
None
Publication
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