Linked Data
ClinVar Variation Id:
1077945
ClinVar RCV Id:
RCV001392703
dbSNP Id:
rs751802421
ExAC:
13:52520558 C / T
gnomAD v2:
13-52520558-C-T
gnomAD v3:
13-51946422-C-T
gnomAD v4:
13-51946422-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51946422C>T , CM000675.2:g.51946422C>T | GRCh38 |
| NC_000013.10:g.52520558C>T , CM000675.1:g.52520558C>T | GRCh37 |
| NC_000013.9:g.51418559C>T | NCBI36 |
| NG_008806.1:g.70073G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*755G>A | ENSP00000489512.2:n.*755G>A | |
| ENST00000673864.2:c.*1666G>A | ENSP00000501045.2:n.*1666G>A | |
| ENST00000674147.2:c.2301G>A | ENSP00000500964.2:p.Thr767= | |
| ENST00000242839.10:c.2922G>A MANE Select | ENSP00000242839.5:p.Thr974= | |
| ENST00000344297.9:c.2301G>A | ENSP00000342559.5:p.Thr767= | |
| ENST00000400366.6:c.2589G>A | ENSP00000383217.3:p.Thr863= | |
| ENST00000448424.7:c.2670G>A | ENSP00000416738.3:p.Thr890= | |
| ENST00000673772.1:c.2688G>A | ENSP00000501168.1:p.Thr896= | |
| ENST00000673867.1:n.1069G>A | ||
| ENST00000674126.1:n.3285G>A | ||
| ENST00000674147.1:c.1857G>A | ENSP00000500964.1:p.Thr619= | |
| ENST00000242839.8:c.2922G>A | ENSP00000242839.4:p.Thr974= | |
| ENST00000344297.8:c.2301G>A | ENSP00000342559.5:p.Thr767= | |
| ENST00000400366.5:c.2589G>A | ENSP00000383217.3:p.Thr863= | |
| ENST00000400370.8:c.1632G>A | ENSP00000383221.3:p.Thr544= | |
| ENST00000418097.7:c.2866-2131G>A | ENSP00000393343.2:n.2866-2131G>A | |
| ENST00000448424.6:c.2688G>A | ENSP00000416738.2:p.Thr896= | |
| ENST00000466629.1:n.142G>A | ||
| ENST00000634296.1:c.883G>A | ||
| ENST00000634308.1:c.*23G>A | ENSP00000489234.1:n.*23G>A | |
| ENST00000634620.1:n.3666G>A | ||
| ENST00000634810.1:n.2267G>A | ||
| ENST00000634844.1:c.2778G>A | ENSP00000489398.1:p.Thr926= | |
| ENST00000635406.1:n.268G>A | ||
| NM_000053.3:c.2922G>A | NP_000044.2:p.Thr974= | |
| NM_001005918.2:c.2301G>A | NP_001005918.1:p.Thr767= | |
| NM_001243182.1:c.2589G>A | NP_001230111.1:p.Thr863= | |
| XM_005266423.2:c.2826G>A | XP_005266480.1:p.Thr942= | |
| XM_005266424.3:c.2826G>A | XP_005266481.1:p.Thr942= | |
| XM_005266427.2:c.2688G>A | XP_005266484.1:p.Thr896= | |
| XM_005266428.1:c.2670G>A | XP_005266485.1:p.Thr890= | |
| XM_005266430.3:c.2922G>A | XP_005266487.1:p.Thr974= | |
| XM_005266431.2:c.2886G>A | XP_005266488.1:p.Thr962= | |
| XM_005266432.2:c.2436G>A | XP_005266489.1:p.Thr812= | |
| XM_006719837.2:c.2826G>A | XP_006719900.1:p.Thr942= | |
| XM_006719838.1:c.738G>A | XP_006719901.1:p.Thr246= | |
| XM_006719839.1:c.738G>A | XP_006719902.1:p.Thr246= | |
| XM_011535117.1:c.2826G>A | XP_011533419.1:p.Thr942= | |
| XM_011535118.1:c.2787G>A | XP_011533420.1:p.Thr929= | |
| XM_011535119.1:c.2922G>A | XP_011533421.1:p.Thr974= | |
| XM_011535120.1:c.2508G>A | XP_011533422.1:p.Thr836= | |
| XM_011535121.1:c.2730+3585G>A | XP_011533423.1:n.2730+3585G>A | |
| XM_011535122.1:c.1590G>A | XP_011533424.1:p.Thr530= | |
| XR_941601.1:n.3141G>A | ||
| XR_941602.1:n.3141G>A | ||
| XR_941603.1:n.3141G>A | ||
| XR_941604.1:n.3141G>A | ||
| NM_001330578.1:c.2688G>A | NP_001317507.1:p.Thr896= | |
| NM_001330579.1:c.2670G>A | NP_001317508.1:p.Thr890= | |
| XM_005266424.4:c.2826G>A | XP_005266481.1:p.Thr942= | |
| XM_005266430.4:c.2922G>A | XP_005266487.1:p.Thr974= | |
| XM_005266431.4:c.2886G>A | XP_005266488.1:p.Thr962= | |
| XM_006719837.3:c.2826G>A | XP_006719900.1:p.Thr942= | |
| XM_011535117.3:c.2826G>A | XP_011533419.1:p.Thr942= | |
| XM_017020627.1:c.2826G>A | XP_016876116.1:p.Thr942= | |
| NM_000053.4:c.2922G>A MANE Select | NP_000044.2:p.Thr974= | |
| NM_001005918.3:c.2301G>A | NP_001005918.1:p.Thr767= | |
| NM_001330579.2:c.2670G>A | NP_001317508.1:p.Thr890= | |
| NM_001243182.2:c.2589G>A | NP_001230111.1:p.Thr863= | |
| NM_001330578.2:c.2688G>A | NP_001317507.1:p.Thr896= |