| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.53794991A= , CM000666.2:g.53794991A= | GRCh38 |
| NC_000004.11:g.54661158A= , CM000666.1:g.54661158A= | GRCh37 |
| NC_000004.10:g.54355915A= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000507166.5:c.1017+369026A= | ENSP00000423325.1:n.1017+369026A= |