| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.3993759T= , CM000665.2:g.3993759T= | GRCh38 |
| NC_000003.11:g.4035443T= , CM000665.1:g.4035443T= | GRCh37 |
| NC_000003.10:g.4010443T= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000448413.5:c.1191+74810A= | ENSP00000404384.1:n.1191+74810A= |