hgvs

Python library to parse, format, validate, normalize, and map sequence variants according to HGVS Nomenclature (https://hgvs-nomenclature.org/).

Tool suite for HGVS variant descriptions

A high-performance HGVS variant nomenclature parser and normalizer written in Rust

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

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.

A Boolean Algebra for Genetic Variants

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

Variant translation library for Clojure

Clojure(Script) library for handling HGVS

HGVS numbering conversions

Mutalyzer API client and command line interface.

Library for DNA parsing / reading etc.

HGVS variant description parser

A liteweight Python parser for HGVS names

Reference tools and datasets for heavy goods vehicle (HGV) navigation workflows and map data preparation.

REST Interface for VariantValidator. Includes docker container

Terminal-based AI assistant for interpreting genetic variants, combining Ensembl VEP, ClinVar, and MCP tool-calling to turn variant identifiers into readable clinical and biological annotations.

Lightweight HGVS variant parser

HGVS variant name parsing and generation