[ensembl-dev] annotate variants on refseq transcripts through rest api ?

[Caleb Davis]

Hi dev-ensembl,

I would like to annotate intron numbers with respect to refseq
transcripts for genomic changes  through the rest api, but I can't figure
out how. It looks like I can do what I want through the command line VEP
script using --refseq, but I would prefer to use the API if at all
possible. Please advise.

Many thanks, --Caleb
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