Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.23806053A= , CM000675.2:g.23806053A= | GRCh38 |
| NC_000013.10:g.24380192A= , CM000675.1:g.24380192A= | GRCh37 |
| NC_000013.9:g.23278192A= | NCBI36 |
| NG_052977.1:g.88396T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005932.4:c.1745T= MANE Select | NP_005923.3:p.Leu582= |
| ENST00000382172.4:c.1745T= MANE Select | ENSP00000371607.3:p.Leu582= |
| NM_005932.3:c.1745T= | NP_005923.2:p.Leu582= |
| ENST00000382172.3:c.1745T= | ENSP00000371607.3:p.Leu582= |
| XM_011535097.1:c.1559T= | XP_011533399.1:p.Leu520= |
| XM_011535097.2:c.1559T= | XP_011533399.1:p.Leu520= |
| XM_011535098.1:c.1745T= | XP_011533400.1:p.Leu582= |
| XM_011535098.3:c.1745T= | XP_011533400.1:p.Leu582= |