How do I search for SNVs/indels by genomic positions?

Mastermind supports GRCh37 and GRCh38 searches for SNVs/indels. Variants can be entered directly in the search box as shown below in GRCh37 and GRCh38, respectively:
NC_000001.10:g.94508323G>A
NC_000001.11:g.94042767G>A

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To search for genomic coordinates in Mastermind, enter them in the search bar with the appropriate sequence identifier or modify the URL directly as in the example link below:

https://mastermind.genomenon.com/articles?mutation=(add chromosome here):g.94508323G>A
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Where (add chromosome here) can be taken from the list below and substituted into the URL.

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See table here

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