Linked Data
dbSNP Id:
rs868407759
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.65868569C>A , CM000673.2:g.65868569C>A | GRCh38 |
| NC_000011.9:g.65636040C>A , CM000673.1:g.65636040C>A | GRCh37 |
| NC_000011.8:g.65392616C>A | NCBI36 |
| NG_012304.2:g.9366G>T | |
| NG_053116.1:g.13508C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307998.11:c.788G>T MANE Select | ENSP00000309953.6:p.Gly263Val | |
| ENST00000307998.10:c.788G>T | ENSP00000309953.6:p.Gly263Val | |
| ENST00000526628.5:n.1354G>T | ||
| ENST00000527969.1:n.1473G>T | ||
| ENST00000528176.5:c.788G>T | ENSP00000434151.1:p.Gly263Val | |
| ENST00000531005.5:n.1782G>T | ||
| ENST00000531972.5:c.788G>T | ENSP00000435295.1:p.Gly263Val | |
| ENST00000532084.5:n.214G>T | ||
| NM_016938.4:c.788G>T | NP_058634.4:p.Gly263Val | |
| NR_037718.1:n.1047G>T | ||
| NM_016938.5:c.788G>T MANE Select | NP_058634.4:p.Gly263Val | |
| NR_037718.2:n.913G>T |