Linked Data
ClinVar Variation Id:
254768
dbSNP Id:
rs145887771
ExAC:
13:52516532 G / A
gnomAD v2:
13-52516532-G-A
gnomAD v3:
13-51942396-G-A
gnomAD v4:
13-51942396-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51942396G>A , CM000675.2:g.51942396G>A | GRCh38 |
| NC_000013.10:g.52516532G>A , CM000675.1:g.52516532G>A | GRCh37 |
| NC_000013.9:g.51414533G>A | NCBI36 |
| NG_008806.1:g.74099C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*1052C>T | ENSP00000489512.2:n.*1052C>T | |
| ENST00000673864.2:c.*2146C>T | ENSP00000501045.2:n.*2146C>T | |
| ENST00000674147.2:c.2781C>T | ENSP00000500964.2:p.Pro927= | |
| ENST00000242839.10:c.3402C>T MANE Select | ENSP00000242839.5:p.Pro1134= | |
| ENST00000344297.9:c.2781C>T | ENSP00000342559.5:p.Pro927= | |
| ENST00000400366.6:c.3069C>T | ENSP00000383217.3:p.Pro1023= | |
| ENST00000448424.7:c.3150C>T | ENSP00000416738.3:p.Pro1050= | |
| ENST00000673772.1:c.3168C>T | ENSP00000501168.1:p.Pro1056= | |
| ENST00000673867.1:n.3541C>T | ||
| ENST00000674126.1:n.3765C>T | ||
| ENST00000674147.1:c.2337C>T | ENSP00000500964.1:p.Pro779= | |
| ENST00000242839.8:c.3402C>T | ENSP00000242839.4:p.Pro1134= | |
| ENST00000344297.8:c.2781C>T | ENSP00000342559.5:p.Pro927= | |
| ENST00000400366.5:c.3069C>T | ENSP00000383217.3:p.Pro1023= | |
| ENST00000400370.8:c.2112C>T | ENSP00000383221.3:p.Pro704= | |
| ENST00000418097.7:c.3207C>T | ENSP00000393343.2:p.Pro1069= | |
| ENST00000448424.6:c.3168C>T | ENSP00000416738.2:p.Pro1056= | |
| ENST00000634296.1:c.1180C>T | ||
| ENST00000634308.1:c.*503C>T | ENSP00000489234.1:n.*503C>T | |
| ENST00000634620.1:n.4146C>T | ||
| ENST00000634810.1:n.2747C>T | ||
| ENST00000634844.1:c.3258C>T | ENSP00000489398.1:p.Pro1086= | |
| NM_000053.3:c.3402C>T | NP_000044.2:p.Pro1134= | |
| NM_001005918.2:c.2781C>T | NP_001005918.1:p.Pro927= | |
| NM_001243182.1:c.3069C>T | NP_001230111.1:p.Pro1023= | |
| XM_005266423.2:c.3306C>T | XP_005266480.1:p.Pro1102= | |
| XM_005266424.3:c.3306C>T | XP_005266481.1:p.Pro1102= | |
| XM_005266427.2:c.3168C>T | XP_005266484.1:p.Pro1056= | |
| XM_005266428.1:c.3150C>T | XP_005266485.1:p.Pro1050= | |
| XM_005266430.3:c.3402C>T | XP_005266487.1:p.Pro1134= | |
| XM_005266431.2:c.3366C>T | XP_005266488.1:p.Pro1122= | |
| XM_005266432.2:c.2916C>T | XP_005266489.1:p.Pro972= | |
| XM_006719837.2:c.3306C>T | XP_006719900.1:p.Pro1102= | |
| XM_006719838.1:c.1218C>T | XP_006719901.1:p.Pro406= | |
| XM_006719839.1:c.1035C>T | XP_006719902.1:p.Pro345= | |
| XM_011535117.1:c.3306C>T | XP_011533419.1:p.Pro1102= | |
| XM_011535118.1:c.3267C>T | XP_011533420.1:p.Pro1089= | |
| XM_011535119.1:c.3219C>T | XP_011533421.1:p.Pro1073= | |
| XM_011535120.1:c.2988C>T | XP_011533422.1:p.Pro996= | |
| XM_011535121.1:c.2889C>T | XP_011533423.1:p.Pro963= | |
| XM_011535122.1:c.2070C>T | XP_011533424.1:p.Pro690= | |
| XR_941601.1:n.3621C>T | ||
| XR_941602.1:n.3621C>T | ||
| XR_941603.1:n.3621C>T | ||
| XR_941604.1:n.3621C>T | ||
| NM_001330578.1:c.3168C>T | NP_001317507.1:p.Pro1056= | |
| NM_001330579.1:c.3150C>T | NP_001317508.1:p.Pro1050= | |
| XM_005266424.4:c.3306C>T | XP_005266481.1:p.Pro1102= | |
| XM_005266430.4:c.3402C>T | XP_005266487.1:p.Pro1134= | |
| XM_005266431.4:c.3366C>T | XP_005266488.1:p.Pro1122= | |
| XM_006719837.3:c.3306C>T | XP_006719900.1:p.Pro1102= | |
| XM_011535117.3:c.3306C>T | XP_011533419.1:p.Pro1102= | |
| XM_017020627.1:c.3306C>T | XP_016876116.1:p.Pro1102= | |
| NM_000053.4:c.3402C>T MANE Select | NP_000044.2:p.Pro1134= | |
| NM_001005918.3:c.2781C>T | NP_001005918.1:p.Pro927= | |
| NM_001330579.2:c.3150C>T | NP_001317508.1:p.Pro1050= | |
| NM_001243182.2:c.3069C>T | NP_001230111.1:p.Pro1023= | |
| NM_001330578.2:c.3168C>T | NP_001317507.1:p.Pro1056= |