Can I map your variant coordinates between different genome assemblies?

We have data presented on GRCh38, GRCh37 and NCBI36, please check the data portal to see what assembly the data is on. If you need variant calls to be in a particular assembly it is best to go to dbSNP, Ensembl or an equivalent archive using their rs numbers as this will provide a definitive mapping.

If an rs number or equivalent is not available there are tools available to map between NCBI36, GRCh37 and GRCh38 from both Ensembl and the NCBI

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