Linked Data
dbSNP Id:
rs772703155
ExAC:
13:52520594 G / C
gnomAD v2:
13-52520594-G-C
gnomAD v3:
13-51946458-G-C
gnomAD v4:
13-51946458-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.51946458G>C , CM000675.2:g.51946458G>C | GRCh38 |
| NC_000013.10:g.52520594G>C , CM000675.1:g.52520594G>C | GRCh37 |
| NC_000013.9:g.51418595G>C | NCBI36 |
| NG_008806.1:g.70037C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000634296.2:c.*719C>G | ENSP00000489512.2:n.*719C>G | |
| ENST00000673864.2:c.*1630C>G | ENSP00000501045.2:n.*1630C>G | |
| ENST00000674147.2:c.2265C>G | ENSP00000500964.2:p.Ser755= | |
| ENST00000242839.10:c.2886C>G MANE Select | ENSP00000242839.5:p.Ser962= | |
| ENST00000344297.9:c.2265C>G | ENSP00000342559.5:p.Ser755= | |
| ENST00000400366.6:c.2553C>G | ENSP00000383217.3:p.Ser851= | |
| ENST00000448424.7:c.2634C>G | ENSP00000416738.3:p.Ser878= | |
| ENST00000673772.1:c.2652C>G | ENSP00000501168.1:p.Ser884= | |
| ENST00000673867.1:n.1033C>G | ||
| ENST00000674126.1:n.3249C>G | ||
| ENST00000674147.1:c.1821C>G | ENSP00000500964.1:p.Ser607= | |
| ENST00000242839.8:c.2886C>G | ENSP00000242839.4:p.Ser962= | |
| ENST00000344297.8:c.2265C>G | ENSP00000342559.5:p.Ser755= | |
| ENST00000400366.5:c.2553C>G | ENSP00000383217.3:p.Ser851= | |
| ENST00000400370.8:c.1596C>G | ENSP00000383221.3:p.Ser532= | |
| ENST00000418097.7:c.2866-2167C>G | ENSP00000393343.2:n.2866-2167C>G | |
| ENST00000448424.6:c.2652C>G | ENSP00000416738.2:p.Ser884= | |
| ENST00000466629.1:n.106C>G | ||
| ENST00000634296.1:c.847C>G | ||
| ENST00000634308.1:c.2672C>G | ENSP00000489234.1:p.Pro891Arg | |
| ENST00000634620.1:n.3630C>G | ||
| ENST00000634810.1:n.2231C>G | ||
| ENST00000634844.1:c.2742C>G | ENSP00000489398.1:p.Ser914= | |
| ENST00000635406.1:n.232C>G | ||
| NM_000053.3:c.2886C>G | NP_000044.2:p.Ser962= | |
| NM_001005918.2:c.2265C>G | NP_001005918.1:p.Ser755= | |
| NM_001243182.1:c.2553C>G | NP_001230111.1:p.Ser851= | |
| XM_005266423.2:c.2790C>G | XP_005266480.1:p.Ser930= | |
| XM_005266424.3:c.2790C>G | XP_005266481.1:p.Ser930= | |
| XM_005266427.2:c.2652C>G | XP_005266484.1:p.Ser884= | |
| XM_005266428.1:c.2634C>G | XP_005266485.1:p.Ser878= | |
| XM_005266430.3:c.2886C>G | XP_005266487.1:p.Ser962= | |
| XM_005266431.2:c.2850C>G | XP_005266488.1:p.Ser950= | |
| XM_005266432.2:c.2400C>G | XP_005266489.1:p.Ser800= | |
| XM_006719837.2:c.2790C>G | XP_006719900.1:p.Ser930= | |
| XM_006719838.1:c.702C>G | XP_006719901.1:p.Ser234= | |
| XM_006719839.1:c.702C>G | XP_006719902.1:p.Ser234= | |
| XM_011535117.1:c.2790C>G | XP_011533419.1:p.Ser930= | |
| XM_011535118.1:c.2751C>G | XP_011533420.1:p.Ser917= | |
| XM_011535119.1:c.2886C>G | XP_011533421.1:p.Ser962= | |
| XM_011535120.1:c.2472C>G | XP_011533422.1:p.Ser824= | |
| XM_011535121.1:c.2730+3549C>G | XP_011533423.1:n.2730+3549C>G | |
| XM_011535122.1:c.1554C>G | XP_011533424.1:p.Ser518= | |
| XR_941601.1:n.3105C>G | ||
| XR_941602.1:n.3105C>G | ||
| XR_941603.1:n.3105C>G | ||
| XR_941604.1:n.3105C>G | ||
| NM_001330578.1:c.2652C>G | NP_001317507.1:p.Ser884= | |
| NM_001330579.1:c.2634C>G | NP_001317508.1:p.Ser878= | |
| XM_005266424.4:c.2790C>G | XP_005266481.1:p.Ser930= | |
| XM_005266430.4:c.2886C>G | XP_005266487.1:p.Ser962= | |
| XM_005266431.4:c.2850C>G | XP_005266488.1:p.Ser950= | |
| XM_006719837.3:c.2790C>G | XP_006719900.1:p.Ser930= | |
| XM_011535117.3:c.2790C>G | XP_011533419.1:p.Ser930= | |
| XM_017020627.1:c.2790C>G | XP_016876116.1:p.Ser930= | |
| NM_000053.4:c.2886C>G MANE Select | NP_000044.2:p.Ser962= | |
| NM_001005918.3:c.2265C>G | NP_001005918.1:p.Ser755= | |
| NM_001330579.2:c.2634C>G | NP_001317508.1:p.Ser878= | |
| NM_001243182.2:c.2553C>G | NP_001230111.1:p.Ser851= | |
| NM_001330578.2:c.2652C>G | NP_001317507.1:p.Ser884= |