Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119916500G>A , CM000663.2:g.119916500G>A | GRCh38 |
| NC_000001.10:g.120459123G>A , CM000663.1:g.120459123G>A | GRCh37 |
| NC_000001.9:g.120260646G>A | NCBI36 |
| NG_008163.1:g.158154C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024408.4:c.6222C>T MANE Select | NP_077719.2:p.Thr2074= |
| ENST00000256646.7:c.6222C>T MANE Select | ENSP00000256646.2:p.Thr2074= |
| NM_024408.3:c.6222C>T | NP_077719.2:p.Thr2074= |
| ENST00000256646.6:c.6222C>T | ENSP00000256646.2:p.Thr2074= |
| XM_005270901.2:c.6105C>T | XP_005270958.1:p.Thr2035= |
| XM_011541519.1:c.6210C>T | XP_011539821.1:p.Thr2070= |
| XM_011541520.1:c.6105C>T | XP_011539822.1:p.Thr2035= |