Open davmlaw opened 3 months ago
A MT variant is only created once, then linked to the allele via both genome builds
So when you search for it, it gives you 2 entries that match on both builds
Since it only jumps for 1 result
I implemented this by making SearchResult hashable/have equality based on Preview - so this is used to finally merge the results from diff genome builds and jump to just 1
ENST00000361381.2(MT-ND4):c.278_279insT NC_012920.1:m.11037_11038insT
Both went straight to the allele page when genome build set to GRCh38, without any warning that the alt was different BUT correct warning was shown when preferred build was GRCh37 (even though variant was imported as GRCh38)