Linked Data
ClinVar Variation Id:
2152193
ClinVar RCV Id:
RCV003061598
dbSNP Id:
rs181388674
gnomAD v3:
13-51950362-C-G
gnomAD v4:
13-51950362-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51950362C>G , CM000675.2:g.51950362C>G | GRCh38 |
| NC_000013.10:g.52524498C>G , CM000675.1:g.52524498C>G | GRCh37 |
| NC_000013.9:g.51422499C>G | NCBI36 |
| NG_008806.1:g.66133G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*318G>C | ENSP00000489512.2:n.*318G>C | |
| ENST00000673864.2:c.*1229G>C | ENSP00000501045.2:n.*1229G>C | |
| ENST00000674147.2:c.1999G>C | ENSP00000500964.2:p.Asp667His | |
| ENST00000242839.10:c.2485G>C MANE Select | ENSP00000242839.5:p.Asp829His | |
| ENST00000344297.9:c.1999G>C | ENSP00000342559.5:p.Asp667His | |
| ENST00000400366.6:c.2152G>C | ENSP00000383217.3:p.Asp718His | |
| ENST00000448424.7:c.2233G>C | ENSP00000416738.3:p.Asp745His | |
| ENST00000673772.1:c.2251G>C | ENSP00000501168.1:p.Asp751His | |
| ENST00000674147.1:c.1555G>C | ENSP00000500964.1:p.Asp519His | |
| ENST00000242839.8:c.2485G>C | ENSP00000242839.4:p.Asp829His | |
| ENST00000344297.8:c.1999G>C | ENSP00000342559.5:p.Asp667His | |
| ENST00000400366.5:c.2152G>C | ENSP00000383217.3:p.Asp718His | |
| ENST00000400370.8:c.1286-201G>C | ENSP00000383221.3:n.1286-201G>C | |
| ENST00000418097.7:c.2485G>C | ENSP00000393343.2:p.Asp829His | |
| ENST00000448424.6:c.2251G>C | ENSP00000416738.2:p.Asp751His | |
| ENST00000634296.1:c.446G>C | ||
| ENST00000634308.1:c.2251G>C | ENSP00000489234.1:p.Asp751His | |
| ENST00000634620.1:n.3283G>C | ||
| ENST00000634810.1:n.1830G>C | ||
| ENST00000634844.1:c.2341G>C | ENSP00000489398.1:p.Asp781His | |
| ENST00000635406.1:n.212-3884G>C | ||
| NM_000053.3:c.2485G>C | NP_000044.2:p.Asp829His | |
| NM_001005918.2:c.1999G>C | NP_001005918.1:p.Asp667His | |
| NM_001243182.1:c.2152G>C | NP_001230111.1:p.Asp718His | |
| XM_005266423.2:c.2389G>C | XP_005266480.1:p.Asp797His | |
| XM_005266424.3:c.2389G>C | XP_005266481.1:p.Asp797His | |
| XM_005266427.2:c.2251G>C | XP_005266484.1:p.Asp751His | |
| XM_005266428.1:c.2233G>C | XP_005266485.1:p.Asp745His | |
| XM_005266430.3:c.2485G>C | XP_005266487.1:p.Asp829His | |
| XM_005266431.2:c.2449G>C | XP_005266488.1:p.Asp817His | |
| XM_005266432.2:c.1999G>C | XP_005266489.1:p.Asp667His | |
| XM_006719837.2:c.2389G>C | XP_006719900.1:p.Asp797His | |
| XM_006719838.1:c.301G>C | XP_006719901.1:p.Asp101His | |
| XM_006719839.1:c.301G>C | XP_006719902.1:p.Asp101His | |
| XM_011535117.1:c.2389G>C | XP_011533419.1:p.Asp797His | |
| XM_011535118.1:c.2485G>C | XP_011533420.1:p.Asp829His | |
| XM_011535119.1:c.2485G>C | XP_011533421.1:p.Asp829His | |
| XM_011535120.1:c.2071G>C | XP_011533422.1:p.Asp691His | |
| XM_011535121.1:c.2485G>C | XP_011533423.1:p.Asp829His | |
| XM_011535122.1:c.1153G>C | XP_011533424.1:p.Asp385His | |
| XR_941601.1:n.2704G>C | ||
| XR_941602.1:n.2704G>C | ||
| XR_941603.1:n.2704G>C | ||
| XR_941604.1:n.2704G>C | ||
| NM_001330578.1:c.2251G>C | NP_001317507.1:p.Asp751His | |
| NM_001330579.1:c.2233G>C | NP_001317508.1:p.Asp745His | |
| XM_005266424.4:c.2389G>C | XP_005266481.1:p.Asp797His | |
| XM_005266430.4:c.2485G>C | XP_005266487.1:p.Asp829His | |
| XM_005266431.4:c.2449G>C | XP_005266488.1:p.Asp817His | |
| XM_006719837.3:c.2389G>C | XP_006719900.1:p.Asp797His | |
| XM_011535117.3:c.2389G>C | XP_011533419.1:p.Asp797His | |
| XM_017020627.1:c.2389G>C | XP_016876116.1:p.Asp797His | |
| NM_000053.4:c.2485G>C MANE Select | NP_000044.2:p.Asp829His | |
| NM_001005918.3:c.1999G>C | NP_001005918.1:p.Asp667His | |
| NM_001330579.2:c.2233G>C | NP_001317508.1:p.Asp745His | |
| NM_001243182.2:c.2152G>C | NP_001230111.1:p.Asp718His | |
| NM_001330578.2:c.2251G>C | NP_001317507.1:p.Asp751His |