General complicating factor: the gene/genomic accession/transcript accession are basically used as "guides" to figure out where the numeric coordinates given should be positioned. In general, chromosome/genomic accession is ignored if a transcript is given. But if a user wants to use the genomic accession as the reference for the genomic coordinates, they need a way of picking a genomic accession manually or from a list of options, and to leave the transcript field blank, because Cool-Seq-Tool will always prefer a transcript over a genomic accession if both are given.
To the extent ^^^ that the chromosome field is now locked down, we can probably also revisit whether it still needs the annoying hover-over that clarifies the kinds of legal inputs.
Originally posted by @jsstevenson in https://github.com/cancervariants/fusion-curation/pull/273#pullrequestreview-2172573887