Linked Data
ClinVar Variation Id:
2201105
dbSNP Id:
rs375436098
ExAC:
10:99359563 G / A
gnomAD v2:
10-99359563-G-A
gnomAD v3:
10-97599806-G-A
gnomAD v4:
10-97599806-G-A
COSMIC:
COSM1203506
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97599806G>A , CM000672.2:g.97599806G>A | GRCh38 |
| NC_000010.10:g.99359563G>A , CM000672.1:g.99359563G>A | GRCh37 |
| NC_000010.9:g.99349553G>A | NCBI36 |
| NG_027922.1:g.20462G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370646.9:c.595G>A MANE Select | ENSP00000359680.4:p.Gly199Ser | |
| ENST00000370642.4:c.5G>A | ||
| ENST00000370646.8:c.595G>A | ENSP00000359680.4:p.Gly199Ser | |
| ENST00000370647.8:c.212-2051G>A | ENSP00000359681.4:n.212-2051G>A | |
| ENST00000370649.3:c.212-2051G>A | ENSP00000359683.3:n.212-2051G>A | |
| ENST00000465608.1:n.1439G>A | ||
| NM_001134670.1:c.212-2051G>A | NP_001128142.1:n.212-2051G>A | |
| NM_138413.3:c.595G>A | NP_612422.2:p.Gly199Ser | |
| NM_138413.4:c.595G>A MANE Select | NP_612422.2:p.Gly199Ser | |
| NM_001134670.2:c.212-2051G>A | NP_001128142.1:n.212-2051G>A |