Dealing with pseudoautosomal (PAR) regions
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Description
@EmmaTudini commented on [Wed Oct 27 2021](https://github.com/SACGF/variantgrid_shariant/issues/62)
These are when transcripts go to both chromosome X and Y. At the moment, we only liftover to chromosome X, but ClinVar, VariantValidator, etc liftover to both and show both chromosomes.
Convert to align with international groups. Particularly important if we start getting coordinates/g.hgvs from labs or export as coordinates/g.hgvs to labs.
Interim step could be to flag alleles with this issue for transparency.
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