v0.2.10

• Fix download for refseq_gene_symbols.txt

v0.2.9: Merge pull request #138 from cancervariants/issue-114

• Query seqrepo the efficient way rather than getting entire sequence and then indexing
• Commented out tokenizers that we are not currently using
• Use gene-normalizer to get GeneSymbolTokens
  • Caching this data in both tokenizer and normalize
• Created a table in UTA called genomic to contain genomic accession data (accession, start/end pos, gene). I created a table since we are unable to index views.

v0.2.8

• Update to latest version of VRSATILE
  • ref_allele_seq --> vrs_ref_allele_seq
• Use classes from gene-normalizer rather than implementing again
• Adding validators to pydantic classes

v0.2.6: Merge pull request #134 from cancervariants/issue-132

• normalize return variation descriptor with text object if query can't be normalized
• toVRS returns a list of variations (Allele or Text)

v0.2.5: Merge pull request #123 from cancervariants/variation

• variant --> variation
• Fix validation checks on c. coordinates (previously did not include cds start)
• implement mane transcript instead of using Clin Gen Allele Registry API
• Add mane transcripts for silent mutations
• Get gene from genomic accession

0.2.4: Merge pull request #112 from cancervariants/issue-106

• Simple insertions for p./c./g. references

v0.2.3: Merge pull request #109 from cancervariants/error-fixes

• Fix TypeError when getting transcripts from gene
• Fix ValueError when getting aliases from SeqRepoDataProxy

v0.2.2: Merge pull request #105 from cancervariants/issue-103

• Add support for protein, transcript, and genomic deletions

v0.2.1: Merge pull request #104 from cancervariants/gene-normalizer

• Instantiate gene-normalizer once in init

v0.2.0: Merge pull request #104 from cancervariants/gene-normalizer

• Support protein delins