# create the translation table after fixing the issue with the variant allele encoding
python /home/darren/Documents/2_repos/serenomica/pgx-engine/scripts/pharmvar_to_translation_table.py \
    data/NAT2-6.2.15/GRCh38/NAT2.NC_000008.11.haplotypes.tsv \
    "NAT2" \
    "chr8"

# create the json (needed to change the saving location)
python /home/darren/Documents/2_repos/serenomica/pgx-engine/scripts/translation_to_json.py \
    temp_NAT2_translation_table.tsv \
    "NAT2" \
    "chr8" \
    "GRCh38" \
    "NC_000008.11"