| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61798436T= , CM000673.2:g.61798436T= | GRCh38 |
| NC_000011.9:g.61565908T= , CM000673.1:g.61565908T= | GRCh37 |
| NC_000011.8:g.61322484T= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000574708.5:c.-55+5408T= | ENSP00000458917.1:n.-55+5408T= |