| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.51200506A= , CM000680.2:g.51200506A= | GRCh38 |
| NC_000018.9:g.48726876A= , CM000680.1:g.48726876A= | GRCh37 |
| NC_000018.8:g.46980874A= | NCBI36 |
| NG_015801.1:g.2176T= |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000591040.1:n.43+17756T= | |
| ENST00000591040.2:c.-108+17756T= | ENSP00000502049.1:n.-108+17756T= |