Linked Data
ClinVar Variation Id:
1021850
ClinVar RCV Id:
RCV001321680
dbSNP Id:
rs537576399
ExAC:
17:45299087 C / G
gnomAD v2:
17-45299087-C-G
gnomAD v3:
17-47221721-C-G
gnomAD v4:
17-47221721-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47221721C>G , CM000679.2:g.47221721C>G | GRCh38 |
| NC_000017.10:g.45299087C>G , CM000679.1:g.45299087C>G | GRCh37 |
| NC_000017.9:g.42654086C>G | NCBI36 |
| NG_052847.1:g.17705C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354968.5:c.353C>G | ENSP00000347055.1:p.Pro118Arg | |
| ENST00000393450.5:c.353C>G MANE Select | ENSP00000377096.1:p.Pro118Arg | |
| ENST00000536623.6:c.353C>G | ENSP00000442375.2:p.Pro118Arg | |
| ENST00000570671.1:c.64C>G | ||
| ENST00000570772.5:c.*139C>G | ENSP00000458194.1:n.*139C>G | |
| ENST00000571981.5:c.*139C>G | ENSP00000459035.1:n.*139C>G | |
| ENST00000572303.1:c.446C>G | ENSP00000461747.1:p.Pro149Arg | |
| ENST00000572316.5:c.353C>G | ENSP00000461570.1:p.Pro118Arg | |
| ENST00000573747.6:c.314-11C>G | ENSP00000460734.1:n.314-11C>G | |
| ENST00000576874.5:c.353C>G | ENSP00000458907.1:p.Pro118Arg | |
| NM_001002841.1:c.353C>G | NP_001002841.1:p.Pro118Arg | |
| NM_002476.2:c.353C>G MANE Select | NP_002467.1:p.Pro118Arg | |
| XM_005257391.3:c.353C>G | XP_005257448.1:p.Pro118Arg | |
| XM_011524838.1:c.353C>G | XP_011523140.1:p.Pro118Arg | |
| XM_011524839.1:c.143C>G | XP_011523141.1:p.Pro48Arg | |
| XM_005257391.5:c.353C>G | XP_005257448.1:p.Pro118Arg | |
| XM_011524839.2:c.446C>G | XP_011523141.2:p.Pro149Arg | |
| XM_017024683.1:c.446C>G | XP_016880172.1:p.Pro149Arg | |
| XM_024450766.1:c.446C>G | XP_024306534.1:p.Pro149Arg | |
| NM_001002841.2:c.353C>G | NP_001002841.1:p.Pro118Arg |