Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.74004497G= , CM000673.2:g.74004497G= | GRCh38 |
| NC_000011.9:g.73715542G= , CM000673.1:g.73715542G= | GRCh37 |
| NC_000011.8:g.73393190G= | NCBI36 |
| NG_011515.1:g.9741C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003356.4:c.630C= MANE Select | NP_003347.1:p.Tyr210= |
| ENST00000314032.9:c.630C= MANE Select | ENSP00000323740.4:p.Tyr210= |
| NM_003356.3:c.630C= | NP_003347.1:p.Tyr210= |
| NM_022803.2:c.630C= | NP_073714.1:p.Tyr210= |
| NM_022803.3:c.630C= | NP_073714.1:p.Tyr210= |
| ENST00000314032.8:c.630C= | ENSP00000323740.4:p.Tyr210= |
| ENST00000426995.2:c.630C= | ENSP00000392143.2:p.Tyr210= |
| XR_950298.1:n.1768+8463G= |