Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153740195T= , CM000685.2:g.153740195T= | GRCh38 |
| NC_000023.10:g.153005649T= , CM000685.1:g.153005649T= | GRCh37 |
| NC_000023.9:g.152658843T= | NCBI36 |
| NG_009022.2:g.20328T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.1592T= MANE Select | NP_000024.2:p.Leu531= |
| ENST00000218104.6:c.1592T= MANE Select | ENSP00000218104.3:p.Leu531= |
| NM_000033.3:c.1592T= | NP_000024.2:p.Leu531= |
| ENST00000218104.5:c.1592T= | ENSP00000218104.3:p.Leu531= |
| ENST00000443684.2:n.595T= | |
| XR_938507.1:n.2064T= | |
| XR_938507.2:n.2064T= |