SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131518491T>A , CM000671.2:g.131518491T>A | GRCh38 |
| NC_000009.11:g.134393878T>A , CM000671.1:g.134393878T>A | GRCh37 |
| NC_000009.10:g.133383699T>A | NCBI36 |
| NG_008896.1:g.20590T>A | |
| NG_008896.2:g.20590T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.1157T>A | ENSP00000343034.7:p.Leu386His | |
| ENST00000404875.7:n.1859T>A | ||
| ENST00000423007.6:c.1376T>A | ENSP00000404119.2:p.Leu459His | |
| ENST00000677295.2:c.*1663T>A | ENSP00000504346.2:n.*1663T>A | |
| ENST00000678264.2:c.*1502T>A | ENSP00000503157.2:n.*1502T>A | |
| ENST00000682070.1:n.1784T>A | ||
| ENST00000682535.1:n.91T>A | ||
| ENST00000682539.1:c.257T>A | ||
| ENST00000682813.1:n.1584T>A | ||
| ENST00000683110.1:n.47T>A | ||
| ENST00000683392.1:n.4066T>A | ||
| ENST00000683712.1:n.1724T>A | ||
| ENST00000683900.1:n.3219T>A | ||
| ENST00000684062.1:n.1985T>A | ||
| ENST00000684579.1:n.3165T>A | ||
| ENST00000684679.1:n.546T>A | ||
| ENST00000341012.12:c.1157T>A | ENSP00000343034.7:p.Leu386His | |
| ENST00000372220.5:c.188T>A | ENSP00000361294.5:p.Leu63His | |
| ENST00000372228.9:c.1385T>A | ENSP00000361302.3:p.Leu462His | |
| ENST00000402686.8:c.1319T>A MANE Select | ENSP00000385797.4:p.Leu440His | |
| ENST00000676640.1:c.1319T>A | ENSP00000503281.1:p.Leu440His | |
| ENST00000676803.1:c.494T>A | ENSP00000503093.1:p.Leu165His | |
| ENST00000676835.1:c.*534T>A | ENSP00000502911.1:n.*534T>A | |
| ENST00000677029.1:c.863T>A | ENSP00000502936.1:p.Leu288His | |
| ENST00000677099.1:c.*1029T>A | ENSP00000504553.1:n.*1029T>A | |
| ENST00000677216.1:c.968T>A | ENSP00000503772.1:p.Leu323His | |
| ENST00000677221.1:n.344T>A | ||
| ENST00000677295.1:c.*696T>A | ENSP00000504346.1:n.*696T>A | |
| ENST00000677444.1:c.1125T>A | ||
| ENST00000677586.1:n.800T>A | ||
| ENST00000677626.1:c.968T>A | ENSP00000503552.1:p.Leu323His | |
| ENST00000677677.1:n.1279T>A | ||
| ENST00000677853.1:c.*327T>A | ENSP00000503488.1:n.*327T>A | |
| ENST00000677983.1:n.408T>A | ||
| ENST00000678202.1:n.339T>A | ||
| ENST00000678264.1:c.*696T>A | ENSP00000503157.1:n.*696T>A | |
| ENST00000678303.1:c.1229T>A | ENSP00000503696.1:p.Leu410His | |
| ENST00000678366.1:c.*1568T>A | ENSP00000504353.1:n.*1568T>A | |
| ENST00000678546.1:c.*1264T>A | ENSP00000503062.1:n.*1264T>A | |
| ENST00000678548.1:c.*1391T>A | ENSP00000503934.1:n.*1391T>A | |
| ENST00000678626.1:n.1016T>A | ||
| ENST00000678733.1:c.400T>A | ||
| ENST00000678739.1:c.*1645T>A | ENSP00000503806.1:n.*1645T>A | |
| ENST00000678795.1:n.406T>A | ||
| ENST00000678833.1:c.*766T>A | ENSP00000503893.1:n.*766T>A | |
| ENST00000678942.1:c.499T>A | ENSP00000504690.1:n.499T>A | |
| ENST00000679023.1:c.1157T>A | ENSP00000503718.1:p.Leu386His | |
| ENST00000679076.1:c.938T>A | ||
| ENST00000679111.1:c.1319T>A | ENSP00000504257.1:p.Leu440His | |
| ENST00000679189.1:c.968T>A | ENSP00000503356.1:p.Leu323His | |
| ENST00000341012.11:c.1157T>A | ENSP00000343034.7:p.Leu386His | |
| ENST00000372220.4:c.182T>A | ENSP00000361294.4:p.Leu61His | |
| ENST00000372228.7:c.1385T>A | ENSP00000361302.3:p.Leu462His | |
| ENST00000402686.7:c.1319T>A | ENSP00000385797.3:p.Leu440His | |
| ENST00000404875.6:c.968T>A | ENSP00000384531.2:p.Leu323His | |
| ENST00000423007.5:c.1319T>A | ENSP00000404119.1:p.Leu440His | |
| ENST00000485278.5:n.1874T>A | ||
| NM_001077365.1:c.1319T>A | NP_001070833.1:p.Leu440His | |
| NM_001077366.1:c.1157T>A | NP_001070834.1:p.Leu386His | |
| NM_001136113.1:c.1319T>A | NP_001129585.1:p.Leu440His | |
| NM_001136114.1:c.968T>A | NP_001129586.1:p.Leu323His | |
| NM_007171.3:c.1385T>A | NP_009102.3:p.Leu462His | |
| XM_005272156.1:c.1385T>A | XP_005272213.1:p.Leu462His | |
| XM_005272158.1:c.1223T>A | XP_005272215.1:p.Leu408His | |
| XM_005272159.1:c.1034T>A | XP_005272216.1:p.Leu345His | |
| XM_005272162.1:c.188T>A | XP_005272219.1:p.Leu63His | |
| XM_006716932.1:c.1034T>A | XP_006716995.1:p.Leu345His | |
| XM_011518140.1:c.1238T>A | XP_011516442.1:p.Leu413His | |
| XM_011518141.1:c.1172T>A | XP_011516443.1:p.Leu391His | |
| XM_011518142.1:c.1076T>A | XP_011516444.1:p.Leu359His | |
| XM_011518143.1:c.1070T>A | XP_011516445.1:p.Leu357His | |
| XM_011518144.1:c.1385T>A | XP_011516446.1:p.Leu462His | |
| XM_011518145.1:c.929T>A | XP_011516447.1:p.Leu310His | |
| XM_011518146.1:c.1070T>A | XP_011516448.1:p.Leu357His | |
| XM_011518147.1:c.257T>A | XP_011516449.1:p.Leu86His | |
| XR_929703.1:n.1561T>A | ||
| NM_001353193.1:c.1385T>A | NP_001340122.1:p.Leu462His | |
| NM_001353194.1:c.1157T>A | NP_001340123.1:p.Leu386His | |
| NM_001353195.1:c.968T>A | NP_001340124.1:p.Leu323His | |
| NM_001353196.1:c.1229T>A | NP_001340125.1:p.Leu410His | |
| NM_001353197.1:c.1223T>A | NP_001340126.1:p.Leu408His | |
| NM_001353198.1:c.1223T>A | NP_001340127.1:p.Leu408His | |
| NM_001353199.1:c.1034T>A | NP_001340128.1:p.Leu345His | |
| NM_001353200.1:c.863T>A | NP_001340129.1:p.Leu288His | |
| NR_148391.1:n.1369T>A | ||
| NR_148392.1:n.1587T>A | ||
| NR_148393.1:n.1369T>A | ||
| NR_148394.1:n.1262T>A | ||
| NR_148395.1:n.1521T>A | ||
| NR_148396.1:n.1155T>A | ||
| NR_148397.1:n.1419T>A | ||
| NR_148398.1:n.1374T>A | ||
| NR_148399.1:n.1761T>A | ||
| NR_148400.1:n.1360T>A | ||
| XM_005272162.3:c.188T>A | XP_005272219.1:p.Leu63His | |
| XM_006716932.2:c.1034T>A | XP_006716995.1:p.Leu345His | |
| XM_011518140.2:c.1238T>A | XP_011516442.1:p.Leu413His | |
| XM_011518141.2:c.1172T>A | XP_011516443.1:p.Leu391His | |
| XM_011518142.2:c.1076T>A | XP_011516444.1:p.Leu359His | |
| XM_011518143.2:c.1070T>A | XP_011516445.1:p.Leu357His | |
| XM_011518145.2:c.929T>A | XP_011516447.1:p.Leu310His | |
| XM_017014205.2:c.188T>A | XP_016869694.1:p.Leu63His | |
| XM_024447380.1:c.188T>A | XP_024303148.1:p.Leu63His | |
| XM_024447381.1:c.494T>A | XP_024303149.1:p.Leu165His | |
| XM_024447382.1:c.188T>A | XP_024303150.1:p.Leu63His | |
| XR_001746160.2:n.1489T>A | ||
| XR_001746162.2:n.1555T>A | ||
| XR_001746164.1:n.1272T>A | ||
| XR_001746166.2:n.1706T>A | ||
| NM_001077365.2:c.1319T>A MANE Select | NP_001070833.1:p.Leu440His | |
| NM_001077366.2:c.1157T>A | NP_001070834.1:p.Leu386His | |
| NM_001136113.2:c.1319T>A | NP_001129585.1:p.Leu440His | |
| NM_001136114.2:c.968T>A | NP_001129586.1:p.Leu323His | |
| NM_001353193.2:c.1385T>A | NP_001340122.2:p.Leu462His | |
| NM_001353194.2:c.1157T>A | NP_001340123.1:p.Leu386His | |
| NM_001353195.2:c.968T>A | NP_001340124.1:p.Leu323His | |
| NM_001353196.2:c.1229T>A | NP_001340125.1:p.Leu410His | |
| NM_001353197.2:c.1223T>A | NP_001340126.2:p.Leu408His | |
| NM_001353198.2:c.1223T>A | NP_001340127.2:p.Leu408His | |
| NM_001353199.2:c.1034T>A | NP_001340128.2:p.Leu345His | |
| NM_001353200.2:c.863T>A | NP_001340129.1:p.Leu288His | |
| NM_001374689.1:c.1307T>A | NP_001361618.1:p.Leu436His | |
| NM_001374690.1:c.1319T>A | NP_001361619.1:p.Leu440His | |
| NM_001374691.1:c.968T>A | NP_001361620.1:p.Leu323His | |
| NM_001374692.1:c.968T>A | NP_001361621.1:p.Leu323His | |
| NM_001374693.1:c.968T>A | NP_001361622.1:p.Leu323His | |
| NM_001374695.1:c.929T>A | NP_001361624.1:p.Leu310His | |
| NM_007171.4:c.1385T>A | NP_009102.4:p.Leu462His | |
| NR_148391.2:n.1353T>A | ||
| NR_148392.2:n.1571T>A | ||
| NR_148393.2:n.1353T>A | ||
| NR_148394.2:n.1246T>A | ||
| NR_148395.2:n.1505T>A | ||
| NR_148396.2:n.1139T>A | ||
| NR_148397.2:n.1403T>A | ||
| NR_148398.2:n.1358T>A | ||
| NR_148399.2:n.1745T>A | ||
| NR_148400.2:n.1344T>A |