Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129822666T= , CM000671.2:g.129822666T= | GRCh38 |
| NC_000009.11:g.132584945T= , CM000671.1:g.132584945T= | GRCh37 |
| NC_000009.10:g.131624766T= | NCBI36 |
| NG_008049.1:g.6497A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.359A= MANE Select | ENSP00000345719.4:p.Tyr120= | |
| ENST00000651202.1:c.455A= | ENSP00000498222.1:p.Tyr152= | |
| ENST00000351698.4:c.359A= | ENSP00000345719.4:p.Tyr120= | |
| ENST00000473084.1:n.378A= | ||
| ENST00000473604.2:n.469A= | ||
| NM_000113.2:c.359A= | NP_000104.1:p.Tyr120= | |
| XR_929731.1:n.519A= | ||
| XR_929731.3:n.387A= | ||
| NM_000113.3:c.359A= MANE Select | NP_000104.1:p.Tyr120= |