Back to catalog
Cortexa research tool·genomics·ncbi_variation
NCBIVariation Spdi Equivalents
Get all equivalent SPDI representations of a variant across different reference sequences and genome assemblies (GRCh37/GRCh38, RefSeqGene, transcript). Given one SPDI, returns the same variant mapped to all available coordinate systems. Useful for liftover between assemblies and cross-referencing variants described on different reference sequences.
AvailableCortexa
Schema
JSON Schema the agent (or your API call) must match.
JSON · 12 lines · 278 chars
Examples (1)
Default NCBIVariation Spdi Equivalents call
public-safeinput
JSON · 3 lines · 16 chars
Expected response keys: success
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_NCBIVariation_spdi_equivalents
- Tool name
- NCBIVariation_spdi_equivalents
- Added
- 2026-05-01 00:58Z
- Tags
- tooluniverse