Linked Data
dbSNP Id:
rs778776159
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90501211A>G , CM000677.2:g.90501211A>G | GRCh38 |
| NC_000015.9:g.91044443A>G , CM000677.1:g.91044443A>G | GRCh37 |
| NC_000015.8:g.88845447A>G | NCBI36 |
| NG_052946.1:g.117971A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268182.10:c.*1103A>G MANE Select | ENSP00000268182.5:n.*1103A>G | |
| ENST00000268182.9:c.*1103A>G | ENSP00000268182.5:n.*1103A>G | |
| ENST00000558957.1:n.2135A>G | ||
| ENST00000561086.1:n.1844A>G | ||
| NM_003870.3:c.*1103A>G | NP_003861.1:n.*1103A>G | |
| XR_001751409.2:n.6206A>G | ||
| NM_003870.4:c.*1103A>G MANE Select | NP_003861.1:n.*1103A>G |