Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153725786T= , CM000685.2:g.153725786T= | GRCh38 |
| NC_000023.10:g.152991241T= , CM000685.1:g.152991241T= | GRCh37 |
| NC_000023.9:g.152644435T= | NCBI36 |
| NG_009022.2:g.5919T= | |
| NG_023231.1:g.3961A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000033.4:c.520T= MANE Select | NP_000024.2:p.Tyr174= |
| ENST00000218104.6:c.520T= MANE Select | ENSP00000218104.3:p.Tyr174= |
| NM_000033.3:c.520T= | NP_000024.2:p.Tyr174= |
| ENST00000218104.5:c.520T= | ENSP00000218104.3:p.Tyr174= |
| XR_938507.1:n.936T= | |
| XR_938507.2:n.936T= |