Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94001955A= , CM000663.2:g.94001955A= | GRCh38 |
| NC_000001.10:g.94467511A= , CM000663.1:g.94467511A= | GRCh37 |
| NC_000001.9:g.94240099A= | NCBI36 |
| NG_009073.1:g.124195T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.6185T= MANE Select | ENSP00000359245.3:p.Val2062= | |
| ENST00000370225.3:c.6185T= | ENSP00000359245.3:p.Val2062= | |
| ENST00000465352.1:n.601T= | ||
| ENST00000536513.5:c.2561T= | ENSP00000439707.2:p.Val854= | |
| NM_000350.2:c.6185T= | NP_000341.2:p.Val2062= | |
| NM_000350.3:c.6185T= MANE Select | NP_000341.2:p.Val2062= |