Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52676305T= , CM000674.2:g.52676305T= | GRCh38 |
| NC_000012.11:g.53070089T= , CM000674.1:g.53070089T= | GRCh37 |
| NC_000012.10:g.51356356T= | NCBI36 |
| NG_008364.1:g.9103A= | |
| NG_008364.2:g.9103A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006121.4:c.1445A= MANE Select | NP_006112.3:p.Tyr482= |
| ENST00000252244.3:c.1445A= MANE Select | ENSP00000252244.3:p.Tyr482= |
| NM_006121.3:c.1445A= | NP_006112.3:p.Tyr482= |
| ENST00000548765.1:n.519A= |