Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42900930C>T , CM000679.2:g.42900930C>T | GRCh38 |
| NC_000017.10:g.41052947C>T , CM000679.1:g.41052947C>T | GRCh37 |
| NC_000017.9:g.38306473C>T | NCBI36 |
| NG_011808.1:g.5133C>T , LRG_147:g.5133C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253801.7:c.54C>T MANE Select | ENSP00000253801.1:p.Tyr18= | |
| ENST00000253801.6:c.54C>T | ENSP00000253801.1:p.Tyr18= | |
| ENST00000585489.1:c.54C>T | ENSP00000466202.1:p.Tyr18= | |
| ENST00000588481.1:n.119C>T | ||
| ENST00000592383.5:c.54C>T | ENSP00000465958.1:p.Tyr18= | |
| NM_000151.3:c.54C>T | NP_000142.2:p.Tyr18= | |
| NM_001270397.1:c.54C>T | NP_001257326.1:p.Tyr18= | |
| NM_000151.4:c.54C>T MANE Select | NP_000142.2:p.Tyr18= | |
| NM_001270397.2:c.54C>T | NP_001257326.1:p.Tyr18= |