H > FUT2*01W.02.02
Allele Information
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Phenotypes
H
Genetic Changes
nt change | aa change | Exon/Intron | HGVS | hg19 | hg38 | rsNum | gnomAD |
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c.385A>T | Exon 2 | chr19:49,206,631 | chr19:48,703,374 |
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c.617T>G | p.Val206Gly | Exon 2 | chr19:49,206,863 | chr19:48,703,606 |
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Sequence
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