Same indel called as different SNVs

General
1

Variants 10-64284-G-GCCCTAA and 10-64284-GCCCTAA-G have the same rsID in gnomadv4.1.0 but they are considered different variants on the site with different allele frequencies. Why are they separately being called an insertion and a deletion? Am I missing something here?

Thanks

2

My understanding is that rsIDs are based on genomic co-ordinate rather than a specific variant, so a single rsID can represent more than one variant.