Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5232998C= , CM000673.2:g.5232998C= | GRCh38 |
| NC_000011.9:g.5254228C= , CM000673.1:g.5254228C= | GRCh37 |
| NC_000011.8:g.5210804C= | NCBI36 |
| NG_000007.3:g.64618G= | |
| NG_063112.2:g.15660G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000519.4:c.410G= MANE Select | NP_000510.1:p.Gly137= |
| ENST00000650601.1:c.410G= MANE Select | ENSP00000497529.1:p.Gly137= |
| NM_000519.3:c.410G= | NP_000510.1:p.Gly137= |
| ENST00000292901.7:c.316-200G= | ENSP00000292901.3:n.316-200G= |
| ENST00000380299.3:c.410G= | ENSP00000369654.3:p.Gly137= |
| ENST00000417377.1:c.187G= | ENSP00000414741.1:p.Val63= |
| ENST00000643122.1:c.410G= | ENSP00000494708.1:p.Gly137= |