Linked Data
dbSNP Id:
rs1157813385
gnomAD v2:
1-227083235-G-A
gnomAD v3:
1-226895534-G-A
gnomAD v4:
1-226895534-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.226895534G>A , CM000663.2:g.226895534G>A | GRCh38 |
| NC_000001.10:g.227083235G>A , CM000663.1:g.227083235G>A | GRCh37 |
| NC_000001.9:g.225149858G>A | NCBI36 |
| NG_007381.1:g.29963G>A | |
| NG_012825.2:g.2999G>A | |
| NG_007381.2:g.30351G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366779.6:c.1302G>A | ENSP00000355741.2:p.Val434= | |
| ENST00000366782.6:c.1302G>A | ENSP00000355746.2:p.Val434= | |
| ENST00000366783.8:c.1302G>A MANE Select | ENSP00000355747.3:p.Val434= | |
| ENST00000471728.2:n.1940G>A | ||
| ENST00000524196.6:c.1302G>A | ENSP00000429036.2:p.Val434= | |
| ENST00000626989.3:c.1302G>A | ENSP00000486498.2:p.Val434= | |
| ENST00000676467.1:c.*1129G>A | ENSP00000504294.1:n.*1129G>A | |
| ENST00000676747.1:c.1188+1409G>A | ENSP00000503244.1:n.1188+1409G>A | |
| ENST00000676884.1:c.1302G>A | ENSP00000503200.1:p.Val434= | |
| ENST00000676888.1:c.*643G>A | ENSP00000504483.1:n.*643G>A | |
| ENST00000676907.1:c.*881G>A | ENSP00000504410.1:n.*881G>A | |
| ENST00000676945.1:c.1191+1409G>A | ENSP00000504433.1:n.1191+1409G>A | |
| ENST00000677065.1:n.1863G>A | ||
| ENST00000677414.1:c.1302G>A | ENSP00000503116.1:p.Val434= | |
| ENST00000677529.1:n.3032G>A | ||
| ENST00000677596.1:c.*1524G>A | ENSP00000503618.1:n.*1524G>A | |
| ENST00000677599.1:c.1191+1409G>A | ENSP00000503673.1:n.1191+1409G>A | |
| ENST00000677748.1:n.3557G>A | ||
| ENST00000677880.1:c.867G>A | ENSP00000503121.1:p.Val289= | |
| ENST00000678021.1:c.*925G>A | ENSP00000504674.1:n.*925G>A | |
| ENST00000678233.1:c.1302G>A | ENSP00000504728.1:p.Val434= | |
| ENST00000678320.1:c.1203G>A | ENSP00000503680.1:p.Val401= | |
| ENST00000678655.1:c.1092+1409G>A | ENSP00000504230.1:n.1092+1409G>A | |
| ENST00000678706.1:c.*679G>A | ENSP00000503659.1:n.*679G>A | |
| ENST00000678776.1:c.*1439G>A | ENSP00000504624.1:n.*1439G>A | |
| ENST00000678784.1:c.1073-2186G>A | ENSP00000504652.1:n.1073-2186G>A | |
| ENST00000678820.1:c.1089+1409G>A | ENSP00000504138.1:n.1089+1409G>A | |
| ENST00000678835.1:c.*757-2186G>A | ENSP00000504343.1:n.*757-2186G>A | |
| ENST00000679088.1:c.1302G>A | ENSP00000504727.1:p.Val434= | |
| ENST00000679098.1:c.1302G>A | ENSP00000504303.1:p.Val434= | |
| ENST00000366782.5:c.1401G>A | ENSP00000355746.1:p.Val467= | |
| ENST00000366783.7:c.1302G>A | ENSP00000355747.3:p.Val434= | |
| ENST00000422240.6:c.1299G>A | ENSP00000403737.2:p.Val433= | |
| ENST00000471728.1:n.560G>A | ||
| ENST00000472139.2:c.870G>A | ENSP00000427806.1:p.Val290= | |
| ENST00000626989.2:c.1401G>A | ENSP00000486498.1:p.Val467= | |
| NM_000447.2:c.1302G>A | NP_000438.2:p.Val434= | |
| NM_012486.2:c.1299G>A | NP_036618.2:p.Val433= | |
| XM_005273199.2:c.1302G>A | XP_005273256.1:p.Val434= | |
| XM_011544236.1:c.870G>A | XP_011542538.1:p.Val290= | |
| XR_949149.1:n.2036G>A | ||
| XM_005273199.4:c.1302G>A | XP_005273256.1:p.Val434= | |
| XM_017001835.1:c.1302G>A | XP_016857324.1:p.Val434= | |
| XM_017001836.1:c.1299G>A | XP_016857325.1:p.Val433= | |
| XR_001737316.2:n.1478-2186G>A | ||
| XR_001737317.2:n.1478-2186G>A | ||
| XR_001737318.2:n.2017G>A | ||
| XR_001737319.1:n.2360G>A | ||
| XR_001737320.1:n.2357G>A | ||
| XR_001737321.1:n.1852G>A | ||
| XR_949149.2:n.2014G>A | ||
| XR_949150.3:n.2233G>A | ||
| NM_000447.3:c.1302G>A MANE Select | NP_000438.2:p.Val434= | |
| NM_012486.3:c.1299G>A | NP_036618.2:p.Val433= |