Linked Data
dbSNP Id:
rs281860617
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.173314C>G , CM000678.2:g.173314C>G | GRCh38 |
| NC_000016.9:g.223313C>G , CM000678.1:g.223313C>G | GRCh37 |
| NC_000016.8:g.163313C>G | NCBI36 |
| NG_000006.1:g.34177C>G | |
| NG_059186.1:g.1664C>G | |
| NG_059271.1:g.5468C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.285C>G MANE Select | ENSP00000251595.6:p.Asp95Glu | |
| ENST00000251595.10:c.285C>G | ENSP00000251595.6:p.Asp95Glu | |
| ENST00000397806.1:c.189C>G | ENSP00000380908.1:p.Asp63Glu | |
| ENST00000482565.1:n.421C>G | ||
| ENST00000484216.1:n.254C>G | ||
| NM_000517.4:c.285C>G | NP_000508.1:p.Asp95Glu | |
| NM_000517.6:c.285C>G MANE Select | NP_000508.1:p.Asp95Glu |