Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319479T= , CM000673.2:g.6319479T= | GRCh38 |
| NC_000011.9:g.6340709T= , CM000673.1:g.6340709T= | GRCh37 |
| NC_000011.8:g.6297285T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.470A= MANE Select | ENSP00000307292.3:p.Gln157= | |
| ENST00000303927.3:c.470A= | ENSP00000307292.3:p.Gln157= | |
| ENST00000524852.1:n.256A= | ||
| ENST00000530979.1:c.566A= | ENSP00000432047.1:p.Gln189= | |
| ENST00000532354.1:n.492A= | ||
| NM_145040.2:c.470A= | NP_659477.2:p.Gln157= | |
| XR_930997.1:n.720+1259T= | ||
| XR_001748106.1:n.90T= | ||
| XR_242848.4:n.339T= | ||
| NM_145040.3:c.470A= MANE Select | NP_659477.2:p.Gln157= |