Linked Data
dbSNP Id:
rs923079284
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109264426A>G , CM000663.2:g.109264426A>G | GRCh38 |
| NC_000001.10:g.109807048A>G , CM000663.1:g.109807048A>G | GRCh37 |
| NC_000001.9:g.109608571A>G | NCBI36 |
| NG_052669.1:g.19722A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271332.4:c.5290-28A>G MANE Select | ENSP00000271332.3:n.5290-28A>G | |
| ENST00000271332.3:c.5290-28A>G | ENSP00000271332.3:n.5290-28A>G | |
| NM_001408.2:c.5290-28A>G | NP_001399.1:n.5290-28A>G | |
| XM_005270580.3:c.5290-28A>G | XP_005270637.1:n.5290-28A>G | |
| NM_001408.3:c.5290-28A>G MANE Select | NP_001399.1:n.5290-28A>G |