Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169530805T= , CM000663.2:g.169530805T= | GRCh38 |
| NC_000001.10:g.169500043T= , CM000663.1:g.169500043T= | GRCh37 |
| NC_000001.9:g.167766667T= | NCBI36 |
| NG_011806.1:g.60727A= , LRG_553:g.60727A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000130.5:c.5189A= MANE Select | NP_000121.2:p.Tyr1730= |
| ENST00000367797.9:c.5189A= MANE Select | ENSP00000356771.3:p.Tyr1730= |
| NM_000130.4:c.5189A= , LRG_553t1:c.5189A= | NP_000121.2:p.Tyr1730= |
| ENST00000367796.3:c.5204A= | ENSP00000356770.3:p.Tyr1735= |
| ENST00000367797.7:c.5189A= | ENSP00000356771.3:p.Tyr1730= |
| XM_017000660.2:c.4778A= | XP_016856149.1:p.Tyr1593= |