Linked Data
ClinVar Variation Id:
1146571
ClinVar RCV Id:
RCV001485862
dbSNP Id:
rs1408214363
gnomAD v2:
13-52513244-C-T
gnomAD v4:
13-51939108-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51939108C>T , CM000675.2:g.51939108C>T | GRCh38 |
| NC_000013.10:g.52513244C>T , CM000675.1:g.52513244C>T | GRCh37 |
| NC_000013.9:g.51411245C>T | NCBI36 |
| NG_008806.1:g.77387G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*1292G>A | ENSP00000489512.2:n.*1292G>A | |
| ENST00000673864.2:c.*2386G>A | ENSP00000501045.2:n.*2386G>A | |
| ENST00000674147.2:c.3021G>A | ENSP00000500964.2:p.Val1007= | |
| ENST00000242839.10:c.3642G>A MANE Select | ENSP00000242839.5:p.Val1214= | |
| ENST00000344297.9:c.3021G>A | ENSP00000342559.5:p.Val1007= | |
| ENST00000400366.6:c.3309G>A | ENSP00000383217.3:p.Val1103= | |
| ENST00000448424.7:c.3390G>A | ENSP00000416738.3:p.Val1130= | |
| ENST00000673696.1:n.883G>A | ||
| ENST00000673772.1:c.3408G>A | ENSP00000501168.1:p.Val1136= | |
| ENST00000673867.1:n.3781G>A | ||
| ENST00000673923.1:n.508G>A | ||
| ENST00000674147.1:c.2577G>A | ENSP00000500964.1:p.Val859= | |
| ENST00000242839.8:c.3642G>A | ENSP00000242839.4:p.Val1214= | |
| ENST00000344297.8:c.3021G>A | ENSP00000342559.5:p.Val1007= | |
| ENST00000400366.5:c.3309G>A | ENSP00000383217.3:p.Val1103= | |
| ENST00000400370.8:c.2352G>A | ENSP00000383221.3:p.Val784= | |
| ENST00000418097.7:c.3447G>A | ENSP00000393343.2:p.Val1149= | |
| ENST00000448424.6:c.3408G>A | ENSP00000416738.2:p.Val1136= | |
| ENST00000634296.1:c.1420G>A | ||
| ENST00000634308.1:c.*743G>A | ENSP00000489234.1:n.*743G>A | |
| ENST00000634620.1:n.4386G>A | ||
| ENST00000634810.1:n.2987G>A | ||
| ENST00000634844.1:c.3498G>A | ENSP00000489398.1:p.Val1166= | |
| NM_000053.3:c.3642G>A | NP_000044.2:p.Val1214= | |
| NM_001005918.2:c.3021G>A | NP_001005918.1:p.Val1007= | |
| NM_001243182.1:c.3309G>A | NP_001230111.1:p.Val1103= | |
| XM_005266423.2:c.3546G>A | XP_005266480.1:p.Val1182= | |
| XM_005266424.3:c.3546G>A | XP_005266481.1:p.Val1182= | |
| XM_005266427.2:c.3408G>A | XP_005266484.1:p.Val1136= | |
| XM_005266428.1:c.3390G>A | XP_005266485.1:p.Val1130= | |
| XM_005266430.3:c.3642G>A | XP_005266487.1:p.Val1214= | |
| XM_005266431.2:c.3606G>A | XP_005266488.1:p.Val1202= | |
| XM_005266432.2:c.3156G>A | XP_005266489.1:p.Val1052= | |
| XM_006719837.2:c.3546G>A | XP_006719900.1:p.Val1182= | |
| XM_006719838.1:c.1458G>A | XP_006719901.1:p.Val486= | |
| XM_006719839.1:c.1275G>A | XP_006719902.1:p.Val425= | |
| XM_011535117.1:c.3546G>A | XP_011533419.1:p.Val1182= | |
| XM_011535118.1:c.3507G>A | XP_011533420.1:p.Val1169= | |
| XM_011535119.1:c.3459G>A | XP_011533421.1:p.Val1153= | |
| XM_011535120.1:c.3228G>A | XP_011533422.1:p.Val1076= | |
| XM_011535121.1:c.3129G>A | XP_011533423.1:p.Val1043= | |
| XM_011535122.1:c.2310G>A | XP_011533424.1:p.Val770= | |
| XR_941601.1:n.3861G>A | ||
| XR_941602.1:n.3861G>A | ||
| XR_941603.1:n.3861G>A | ||
| XR_941604.1:n.3861G>A | ||
| NM_001330578.1:c.3408G>A | NP_001317507.1:p.Val1136= | |
| NM_001330579.1:c.3390G>A | NP_001317508.1:p.Val1130= | |
| XM_005266424.4:c.3546G>A | XP_005266481.1:p.Val1182= | |
| XM_005266430.4:c.3642G>A | XP_005266487.1:p.Val1214= | |
| XM_005266431.4:c.3606G>A | XP_005266488.1:p.Val1202= | |
| XM_006719837.3:c.3546G>A | XP_006719900.1:p.Val1182= | |
| XM_011535117.3:c.3546G>A | XP_011533419.1:p.Val1182= | |
| XM_017020627.1:c.3546G>A | XP_016876116.1:p.Val1182= | |
| NM_000053.4:c.3642G>A MANE Select | NP_000044.2:p.Val1214= | |
| NM_001005918.3:c.3021G>A | NP_001005918.1:p.Val1007= | |
| NM_001330579.2:c.3390G>A | NP_001317508.1:p.Val1130= | |
| NM_001243182.2:c.3309G>A | NP_001230111.1:p.Val1103= | |
| NM_001330578.2:c.3408G>A | NP_001317507.1:p.Val1136= |