| HGVS | Genome Assembly | 
|---|---|
| NC_000003.12:g.169764844C>T , CM000665.2:g.169764844C>T | GRCh38 | 
| NC_000003.11:g.169482632C>T , CM000665.1:g.169482632C>T | GRCh37 | 
| NC_000003.10:g.170965326C>T | NCBI36 | 
| NG_016363.1:g.5217G>A , LRG_347:g.5217G>A | 
| HGVS | Amino-acid Change | 
|---|---|
| NR_001566.1:n.217G>A , LRG_347t1:n.217G>A |