Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180654801A>C , CM000665.2:g.180654801A>C | GRCh38 |
| NC_000003.11:g.180372589A>C , CM000665.1:g.180372589A>C | GRCh37 |
| NC_000003.10:g.181855283A>C | NCBI36 |
| NG_029581.1:g.29695T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_181426.2:c.891T>G MANE Select | NP_852091.1:p.Tyr297Ter |
| ENST00000476379.6:c.891T>G MANE Select | ENSP00000417960.2:p.Tyr297Ter |
| NM_181426.1:c.891T>G | NP_852091.1:p.Tyr297Ter |
| ENST00000442201.6:c.891T>G | ENSP00000405708.2:p.Tyr297Ter |
| ENST00000476379.5:c.891T>G | ENSP00000417960.1:p.Tyr297Ter |
| ENST00000650641.1:n.818-2535T>G | |
| ENST00000650889.1:n.1063T>G | |
| ENST00000651046.1:c.739-2535T>G | ENSP00000499175.1:n.739-2535T>G |
| ENST00000651818.1:n.881-2535T>G | |
| ENST00000652024.1:n.830-2535T>G | |
| ENST00000652408.1:n.1028T>G |