Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319464A= , CM000673.2:g.6319464A= | GRCh38 |
| NC_000011.9:g.6340694A= , CM000673.1:g.6340694A= | GRCh37 |
| NC_000011.8:g.6297270A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.485T= MANE Select | ENSP00000307292.3:p.Val162= | |
| ENST00000303927.3:c.485T= | ENSP00000307292.3:p.Val162= | |
| ENST00000524852.1:n.271T= | ||
| ENST00000530979.1:c.581T= | ENSP00000432047.1:p.Val194= | |
| ENST00000532354.1:n.507T= | ||
| NM_145040.2:c.485T= | NP_659477.2:p.Val162= | |
| XR_930997.1:n.720+1244A= | ||
| XR_001748106.1:n.75A= | ||
| XR_242848.4:n.324A= | ||
| NM_145040.3:c.485T= MANE Select | NP_659477.2:p.Val162= |