v0.4.0a7: Merge pull request #302 from cancervariants/staging

• build: update uta tools + other dependencies
• fix: gnomad_vcf_to_protein getting ref/alt values

v0.4.0a6: Merge pull request #297 from cancervariants/staging

• feat: add endpoint for vrs-python _to_hgvs method

v0.4.0a5: Merge pull request #293 from cancervariants/staging

• Switch request body for /translate_to to use pydantic.BaseModel so users can test out the endpoint on the UI

v0.4.0a4: Merge pull request #290 from cancervariants/staging

• Add endpoint (/translate_to) for vrs-python's translate_to method

v0.4.0a3: Merge pull request #286 from cancervariants/issue-285

• Add parsed_to_abs_cnv endpoint to allow parsed ClinVar Copy Number Gain/Loss to be translated to VRS Absolute Copy Number variation

v0.4.0a2: Merge pull request #278 from cancervariants/staging

• Adds relative_cnv option to hgvs_dup_del_mode
  • Default characteristics for HGVS Dup Del Mode updated
• /to_canonical_variation parameters added
  • do_liftover: Whether or not to liftover 37 to 38
  • hgvs_dup_del_mode: Set to determine the VRS variation model used
    • baseline_copies is required when hgvs_dup_del_mode=absolute_cnv
    • relative_copy_class is optional when hgvs_dup_del_mode=relative_cnv

v0.4.0a1: Merge pull request #275 from cancervariants/staging

• CNVs use SequenceLocation as the subject
• /toVRS --> /to_vrs
• Add fastapi tags
• Add initial /to_canonical_variation endpoint for HGVS/SPDI

v0.3.0: Merge pull request #259 from cancervariants/staging

• HGVS to relative / absolute copy number endpoints
• Remove unused methods from validator (human / concise description)
• Use uta-tools to handle MANE transcript work

v0.2.22

• Bump jupyter-server from 1.13.5 to 1.15.4

v0.2.21

• Add vrs-python's translate_from method (hgvs/spdi/beacon/gnomad --> VRS Allele object)