ABO > ABO*cisAB.02
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.526C>G | p.Arg176Gly | Exon 7 |
|
chr9:136,131,592 | chr9:133,256,176 |
|
|
| c.657C>T | Exon 7 |
|
chr9:136,131,461 | chr9:133,256,045 |
|
||
| c.703G>A | p.Gly235Ser | Exon 7 |
|
chr9:136,131,415 | chr9:133,255,999 |
|
|
| c.803G>C | p.Gly268Ala | Exon 7 |
|
chr9:136,131,315 | chr9:133,255,899 |
|
Sequence
None
Publication
None