Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911057G= , CM000679.2:g.42911057G= | GRCh38 |
| NC_000017.10:g.41063074G= , CM000679.1:g.41063074G= | GRCh37 |
| NC_000017.9:g.38316600G= | NCBI36 |
| NG_011808.1:g.15260G= , LRG_147:g.15260G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.705G= MANE Select | ENSP00000253801.1:p.Leu235= | |
| ENST00000253801.6:c.705G= | ENSP00000253801.1:p.Leu235= | |
| ENST00000585489.1:c.*97G= | ENSP00000466202.1:n.*97G= | |
| ENST00000592383.5:c.*97G= | ENSP00000465958.1:n.*97G= | |
| NM_000151.3:c.705G= | NP_000142.2:p.Leu235= | |
| NM_001270397.1:c.*97G= | NP_001257326.1:n.*97G= | |
| NM_000151.4:c.705G= MANE Select | NP_000142.2:p.Leu235= | |
| NM_001270397.2:c.*97G= | NP_001257326.1:n.*97G= |