Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97611568A= , CM000672.2:g.97611568A= | GRCh38 |
| NC_000010.10:g.99371325A= , CM000672.1:g.99371325A= | GRCh37 |
| NC_000010.9:g.99361315A= | NCBI36 |
| NG_027922.1:g.32224A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370646.9:c.893A= MANE Select | ENSP00000359680.4:p.Tyr298= | |
| ENST00000370646.8:c.893A= | ENSP00000359680.4:p.Tyr298= | |
| ENST00000370647.8:c.404A= | ENSP00000359681.4:p.Tyr135= | |
| ENST00000370649.3:c.345+9578A= | ENSP00000359683.3:n.345+9578A= | |
| NM_001134670.1:c.404A= | NP_001128142.1:p.Tyr135= | |
| NM_138413.3:c.893A= | NP_612422.2:p.Tyr298= | |
| NM_138413.4:c.893A= MANE Select | NP_612422.2:p.Tyr298= | |
| NM_001134670.2:c.404A= | NP_001128142.1:p.Tyr135= |