| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.73404186G>A , CM000666.2:g.73404186G>A | GRCh38 |
| NC_000004.11:g.74269903G>A , CM000666.1:g.74269903G>A | GRCh37 |
| NC_000004.10:g.74488767G>A | NCBI36 |
| NG_009291.1:g.4932G>A |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000441319.5:c.48-183G>A | ENSP00000392541.1:n.48-183G>A |