Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153737205T>C , CM000685.2:g.153737205T>C | GRCh38 |
| NC_000023.10:g.153002659T>C , CM000685.1:g.153002659T>C | GRCh37 |
| NC_000023.9:g.152655853T>C | NCBI36 |
| NG_009022.2:g.17338T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.1442T>C MANE Select | NP_000024.2:p.Ile481Thr |
| ENST00000218104.6:c.1442T>C MANE Select | ENSP00000218104.3:p.Ile481Thr |
| NM_000033.3:c.1442T>C | NP_000024.2:p.Ile481Thr |
| ENST00000218104.5:c.1442T>C | ENSP00000218104.3:p.Ile481Thr |
| ENST00000443684.2:n.445T>C | |
| XR_938507.1:n.1914T>C | |
| XR_938507.2:n.1914T>C |