| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71110074G>A , CM000664.2:g.71110074G>A | GRCh38 |
| NC_000002.11:g.71337204G>A , CM000664.1:g.71337204G>A | GRCh37 |
| NC_000002.10:g.71190712G>A | NCBI36 |
| NG_008977.1:g.25191C>T |
| HGVS | Amino-acid Change |
|---|---|
| NM_032601.4:c.427C>T MANE Select | NP_115990.3:p.Arg143Cys |
| ENST00000244217.6:c.427C>T MANE Select | ENSP00000244217.5:p.Arg143Cys |
| NM_032601.3:c.427C>T | NP_115990.3:p.Arg143Cys |
| ENST00000244217.5:c.427C>T | ENSP00000244217.5:p.Arg143Cys |
| ENST00000413592.5:c.133C>T | ENSP00000391140.1:p.Arg45Cys |
| ENST00000462609.2:n.373C>T | |
| XM_005264613.2:c.265C>T | XP_005264670.1:p.Arg89Cys |
| XR_939729.1:n.592C>T | |
| XR_939729.2:n.592C>T |