| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10141751T>G , CM000665.2:g.10141751T>G | GRCh38 |
| NC_000003.11:g.10183435T>G , CM000665.1:g.10183435T>G | GRCh37 |
| NC_000003.10:g.10158435T>G | NCBI36 |
| NG_008212.3:g.5117T>G , LRG_322:g.5117T>G |
| HGVS | Amino-acid Change |
|---|---|
| NM_000551.3:c.-97T>G , LRG_322t1:c.-97T>G | NP_000542.1:n.-97T>G |
| NM_001354723.1:c.-97T>G | NP_001341652.1:n.-97T>G |
| NM_198156.2:c.-97T>G | NP_937799.1:n.-97T>G |
| ENST00000256474.2:c.-97T>G | ENSP00000256474.2:n.-97T>G |