| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5227098T>A , CM000673.2:g.5227098T>A | GRCh38 |
| NC_000011.9:g.5248328T>A , CM000673.1:g.5248328T>A | GRCh37 |
| NC_000011.8:g.5204904T>A | NCBI36 |
| NG_000007.3:g.70518A>T | |
| NG_059281.1:g.4974A>T |
| HGVS | Amino-acid Change |
|---|---|
| ENST00000380315.2:c.-18-59A>T | ENSP00000369671.2:n.-18-59A>T |
| ENST00000647020.1:c.-77A>T | ENSP00000494175.1:n.-77A>T |