Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312797T>G , CM000673.2:g.118312797T>G | GRCh38 |
| NC_000011.9:g.118183512T>G , CM000673.1:g.118183512T>G | GRCh37 |
| NC_000011.8:g.117688722T>G | NCBI36 |
| NG_007383.1:g.13218T>G , LRG_38:g.13218T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.283T>G MANE Select | ENSP00000354566.4:p.Tyr95Asp | |
| ENST00000361763.8:c.283T>G | ENSP00000354566.4:p.Tyr95Asp | |
| ENST00000526146.5:n.829T>G | ||
| ENST00000528435.5:n.836T>G | ||
| ENST00000528600.1:c.265T>G | ENSP00000433975.1:p.Tyr89Asp | |
| ENST00000529713.5:n.389T>G | ||
| ENST00000531913.1:n.654T>G | ||
| NM_000733.3:c.283T>G , LRG_38t1:c.283T>G | NP_000724.1:p.Tyr95Asp | |
| NM_000733.4:c.283T>G MANE Select | NP_000724.1:p.Tyr95Asp |