Linked Data
ClinVar Variation Id:
262475
dbSNP Id:
rs144458131
ExAC:
2:127808084 G / A
gnomAD v2:
2-127808084-G-A
gnomAD v3:
2-127050508-G-A
gnomAD v4:
2-127050508-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.127050508G>A , CM000664.2:g.127050508G>A | GRCh38 |
| NC_000002.11:g.127808084G>A , CM000664.1:g.127808084G>A | GRCh37 |
| NC_000002.10:g.127524554G>A | NCBI36 |
| NG_012042.1:g.61781C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352848.8:c.1170C>T | ENSP00000315284.4:p.His390= | |
| ENST00000316724.10:c.1587C>T MANE Select | ENSP00000316779.5:p.His529= | |
| ENST00000259238.8:c.1299C>T | ENSP00000259238.4:p.His433= | |
| ENST00000316724.9:c.1587C>T | ENSP00000316779.5:p.His529= | |
| ENST00000346226.7:c.1362C>T | ENSP00000315411.3:p.His454= | |
| ENST00000348750.8:c.1035C>T | ENSP00000259237.5:p.His345= | |
| ENST00000351659.7:c.1326C>T | ENSP00000315388.3:p.His442= | |
| ENST00000352848.7:c.1170C>T | ENSP00000315284.4:p.His390= | |
| ENST00000357970.7:c.1458C>T | ENSP00000350654.3:p.His486= | |
| ENST00000376113.6:c.1080C>T | ENSP00000365281.2:p.His360= | |
| ENST00000393040.7:c.1254C>T | ENSP00000376760.3:p.His418= | |
| ENST00000393041.7:c.1233C>T | ENSP00000376761.3:p.His411= | |
| ENST00000409400.1:c.1125C>T | ENSP00000386797.1:p.His375= | |
| ENST00000462958.5:n.4453C>T | ||
| ENST00000466111.5:n.761C>T | ||
| ENST00000484253.1:n.772C>T | ||
| NM_004305.3:c.1170C>T | NP_004296.1:p.His390= | |
| NM_139343.2:c.1587C>T | NP_647593.1:p.His529= | |
| NM_139344.2:c.1458C>T | NP_647594.1:p.His486= | |
| NM_139345.2:c.1326C>T | NP_647595.1:p.His442= | |
| NM_139346.2:c.1299C>T | NP_647596.1:p.His433= | |
| NM_139347.2:c.1362C>T | NP_647597.1:p.His454= | |
| NM_139348.2:c.1254C>T | NP_647598.1:p.His418= | |
| NM_139349.2:c.1233C>T | NP_647599.1:p.His411= | |
| NM_139350.2:c.1125C>T | NP_647600.1:p.His375= | |
| NM_139351.2:c.1035C>T | NP_647601.1:p.His345= | |
| XM_005263642.2:c.1632C>T | XP_005263699.1:p.His544= | |
| XM_005263643.2:c.1539C>T | XP_005263700.1:p.His513= | |
| XM_005263644.2:c.1494C>T | XP_005263701.1:p.His498= | |
| XM_005263645.1:c.1467C>T | XP_005263702.1:p.His489= | |
| XM_005263646.2:c.1218C>T | XP_005263703.1:p.His406= | |
| XM_005263647.2:c.1080C>T | XP_005263704.1:p.His360= | |
| XM_005263648.1:c.963C>T | XP_005263705.1:p.His321= | |
| XM_006712425.2:c.1500C>T | XP_006712488.1:p.His500= | |
| XM_006712426.2:c.1500C>T | XP_006712489.1:p.His500= | |
| XM_006712427.1:c.1422C>T | XP_006712490.1:p.His474= | |
| XM_006712428.2:c.1392C>T | XP_006712491.1:p.His464= | |
| XM_006712429.2:c.1371C>T | XP_006712492.1:p.His457= | |
| XM_006712430.2:c.1347C>T | XP_006712493.1:p.His449= | |
| XM_006712431.2:c.1302C>T | XP_006712494.1:p.His434= | |
| XM_006712432.2:c.1263C>T | XP_006712495.1:p.His421= | |
| XM_006712433.2:c.1173C>T | XP_006712496.1:p.His391= | |
| XM_006712434.2:c.1128C>T | XP_006712497.1:p.His376= | |
| XM_011510975.1:c.1551C>T | XP_011509277.1:p.His517= | |
| NM_001320632.1:c.1080C>T | NP_001307561.1:p.His360= | |
| NM_001320633.1:c.1218C>T | NP_001307562.1:p.His406= | |
| NM_001320634.1:c.963C>T | NP_001307563.1:p.His321= | |
| NM_001320640.1:c.1347C>T | NP_001307569.1:p.His449= | |
| NM_001320641.1:c.1494C>T | NP_001307570.1:p.His498= | |
| NM_001320642.1:c.1506C>T | NP_001307571.1:p.His502= | |
| XM_005263642.4:c.1632C>T | XP_005263699.1:p.His544= | |
| XM_005263643.4:c.1539C>T | XP_005263700.1:p.His513= | |
| XM_005263645.2:c.1467C>T | XP_005263702.1:p.His489= | |
| XM_006712425.4:c.1500C>T | XP_006712488.1:p.His500= | |
| XM_006712426.4:c.1500C>T | XP_006712489.1:p.His500= | |
| XM_006712427.2:c.1422C>T | XP_006712490.1:p.His474= | |
| XM_006712428.4:c.1392C>T | XP_006712491.1:p.His464= | |
| XM_006712429.4:c.1371C>T | XP_006712492.1:p.His457= | |
| XM_006712431.4:c.1302C>T | XP_006712494.1:p.His434= | |
| XM_006712432.4:c.1263C>T | XP_006712495.1:p.His421= | |
| XM_006712433.4:c.1173C>T | XP_006712496.1:p.His391= | |
| XM_006712434.4:c.1128C>T | XP_006712497.1:p.His376= | |
| XM_011510975.3:c.1551C>T | XP_011509277.1:p.His517= | |
| XM_017003819.1:c.1560C>T | XP_016859308.1:p.His520= | |
| XM_017003820.2:c.1362C>T | XP_016859309.1:p.His454= | |
| XM_017003821.2:c.1257C>T | XP_016859310.1:p.His419= | |
| XM_017003822.2:c.1164C>T | XP_016859311.1:p.His388= | |
| XM_017003823.1:c.1161C>T | XP_016859312.1:p.His387= | |
| XM_017003824.1:c.1092C>T | XP_016859313.1:p.His364= | |
| XM_017003825.1:c.1056C>T | XP_016859314.1:p.His352= | |
| XM_017003826.1:c.1053C>T | XP_016859315.1:p.His351= | |
| XM_017003827.2:c.1048-1875C>T | XP_016859316.1:n.1048-1875C>T | |
| XM_017003828.2:c.1003-1875C>T | XP_016859317.1:n.1003-1875C>T | |
| NM_139343.3:c.1587C>T MANE Select | NP_647593.1:p.His529= | |
| NM_001320632.2:c.1080C>T | NP_001307561.1:p.His360= | |
| NM_001320633.2:c.1218C>T | NP_001307562.1:p.His406= | |
| NM_001320640.2:c.1347C>T | NP_001307569.1:p.His449= | |
| NM_001320641.2:c.1494C>T | NP_001307570.1:p.His498= | |
| NM_004305.4:c.1170C>T | NP_004296.1:p.His390= | |
| NM_139344.3:c.1458C>T | NP_647594.1:p.His486= | |
| NM_139345.3:c.1326C>T | NP_647595.1:p.His442= | |
| NM_139346.3:c.1299C>T | NP_647596.1:p.His433= | |
| NM_139347.3:c.1362C>T | NP_647597.1:p.His454= | |
| NM_139348.3:c.1254C>T | NP_647598.1:p.His418= | |
| NM_139349.3:c.1233C>T | NP_647599.1:p.His411= | |
| NM_139350.3:c.1125C>T | NP_647600.1:p.His375= | |
| NM_139351.3:c.1035C>T | NP_647601.1:p.His345= |