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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.
View JSON schemaExpandCollapse
JSON · 12 lines · 278 chars
Examples (1)
Default NCBIVariation Spdi Equivalents call
Public-safe example · rate-limited
JSON input · 3 lines · 42 chars
Expected response keys: success
Identifiers
- Catalog ID
- tu_NCBIVariation_spdi_equivalents
- Tool name
- NCBIVariation_spdi_equivalents
- Added
- 2026-05-01 00:58Z
- Tags
- tooluniverse