https://github.com/biocommons/hgvs
Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).
https://github.com/biocommons/hgvs
bioinformatics genome-analysis genomics hgvs sequencing transcript variant-analysis variation
Last synced: about 1 month ago
JSON representation
Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).
- Host: GitHub
- URL: https://github.com/biocommons/hgvs
- Owner: biocommons
- License: apache-2.0
- Created: 2017-03-09T22:58:27.000Z (about 9 years ago)
- Default Branch: main
- Last Pushed: 2026-02-10T18:43:09.000Z (about 2 months ago)
- Last Synced: 2026-03-03T14:37:10.215Z (about 1 month ago)
- Topics: bioinformatics, genome-analysis, genomics, hgvs, sequencing, transcript, variant-analysis, variation
- Language: Python
- Homepage: https://hgvs.readthedocs.io/
- Size: 23.8 MB
- Stars: 289
- Watchers: 18
- Forks: 98
- Open Issues: 50
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Metadata Files:
- Readme: README.md
- Changelog: CHANGELOG
- Contributing: CONTRIBUTING.md
- License: LICENSE.txt
- Citation: CITATION.cff
- Codeowners: .github/CODEOWNERS
- Authors: AUTHORS