Tool suite for HGVS variant descriptions

Annotate genomics variations of hg19 by using a BED format database, which construct from NCBI annotation release 104

A Boolean Algebra for Genetic Variants

Variant translation library for Clojure

HGVS variant description parser

Mutalyzer API client and command line interface.

Public repository for VariantValidator project

HGVS variant name parsing and generation

A liteweight Python parser for HGVS names

REST Interface for VariantValidator. Includes docker container

HgvsGo is a program designed for analyzing "c." and "p." HGVS (Human Genome Variation Society) notations for single nucleotide variations (SNVs) and small insertions/deletions (indels) after variant calling. It serves as an alternative to tools like snpEff and VEP.

Clojure(Script) library for handling HGVS

PyGeneBe: A Python client seamlessly integrating with the GeneBe platform, offering efficient annotation of genetic variants through its API, while supporting pandas, VCF file formats, and HGVS parsing

Sequence Variant Nomenclature Parser

Python library to parse, format, validate, normalize, and map sequence variants. `pip install hgvs`

TransVar - multiway annotator for precision medicine

HGVS numbering conversions