Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951781T>G , CM000670.2:g.19951781T>G | GRCh38 |
| NC_000008.10:g.19809292T>G , CM000670.1:g.19809292T>G | GRCh37 |
| NC_000008.9:g.19853572T>G | NCBI36 |
| NG_008855.1:g.17711T>G | |
| NG_008855.2:g.55065T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.262T>G MANE Select | ENSP00000497642.1:p.Tyr88Asp | |
| ENST00000311322.8:c.262T>G | ENSP00000309757.6:p.Tyr88Asp | |
| ENST00000520959.5:c.34T>G | ENSP00000428496.1:p.Tyr12Asp | |
| ENST00000521994.1:n.519T>G | ||
| ENST00000522701.5:c.262T>G | ENSP00000428557.1:p.Tyr88Asp | |
| ENST00000524029.5:c.262T>G | ENSP00000428237.1:p.Tyr88Asp | |
| NM_000237.2:c.262T>G | NP_000228.1:p.Tyr88Asp | |
| NM_000237.3:c.262T>G MANE Select | NP_000228.1:p.Tyr88Asp |