Linked Data
ClinVar Variation Id:
127771
dbSNP Id:
rs587780047
gnomAD v2:
7-6022594-T-C
gnomAD v4:
7-5982963-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5982963T>C , CM000669.2:g.5982963T>C | GRCh38 |
| NC_000007.13:g.6022594T>C , CM000669.1:g.6022594T>C | GRCh37 |
| NC_000007.12:g.5989120T>C | NCBI36 |
| NG_008466.1:g.31144A>G , LRG_161:g.31144A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*1431A>G | ENSP00000514615.2:n.*1431A>G | |
| ENST00000699840.2:c.2032A>G | ENSP00000514638.2:p.Ile678Val | |
| ENST00000699930.2:c.1927A>G | ENSP00000514695.2:p.Ile643Val | |
| ENST00000406569.8:c.1678+4124A>G | ENSP00000514464.1:n.1678+4124A>G | |
| ENST00000644110.2:c.*1629A>G | ENSP00000496392.2:n.*1629A>G | |
| ENST00000699752.1:c.1879A>G | ENSP00000514561.1:p.Ile627Val | |
| ENST00000699753.1:c.*1456A>G | ENSP00000514562.1:n.*1456A>G | |
| ENST00000699754.1:c.1837A>G | ENSP00000514563.1:p.Ile613Val | |
| ENST00000699755.1:c.*1434A>G | ENSP00000514564.1:n.*1434A>G | |
| ENST00000699756.1:c.*1622A>G | ENSP00000514565.1:n.*1622A>G | |
| ENST00000699757.1:c.*1292A>G | ENSP00000514566.1:n.*1292A>G | |
| ENST00000699758.1:c.*1292A>G | ENSP00000514567.1:n.*1292A>G | |
| ENST00000699759.1:n.2889A>G | ||
| ENST00000699760.1:c.1717A>G | ENSP00000514568.1:p.Ile573Val | |
| ENST00000699761.1:c.1630A>G | ENSP00000514569.1:p.Ile544Val | |
| ENST00000699762.1:c.1462A>G | ENSP00000514570.1:p.Ile488Val | |
| ENST00000699763.1:c.*1125A>G | ENSP00000514571.1:n.*1125A>G | |
| ENST00000699764.1:c.*353A>G | ENSP00000514572.1:n.*353A>G | |
| ENST00000699765.1:c.*1131A>G | ENSP00000514573.1:n.*1131A>G | |
| ENST00000699766.1:c.2035A>G | ENSP00000514574.1:p.Ile679Val | |
| ENST00000699767.1:c.2035A>G | ENSP00000514575.1:p.Ile679Val | |
| ENST00000699768.1:c.2035A>G | ENSP00000514576.1:p.Ile679Val | |
| ENST00000699811.1:c.1630A>G | ENSP00000514614.1:p.Ile544Val | |
| ENST00000699813.1:n.2148A>G | ||
| ENST00000699814.1:c.1658A>G | ||
| ENST00000699815.1:c.*1566A>G | ENSP00000514616.1:n.*1566A>G | |
| ENST00000699816.1:c.*925A>G | ENSP00000514617.1:n.*925A>G | |
| ENST00000699817.1:c.*1629A>G | ENSP00000514618.1:n.*1629A>G | |
| ENST00000699818.1:c.1630A>G | ENSP00000514619.1:p.Ile544Val | |
| ENST00000699819.1:c.*1192A>G | ENSP00000514620.1:n.*1192A>G | |
| ENST00000699820.1:c.1173A>G | ENSP00000514621.1:p.Ser391= | |
| ENST00000699821.1:c.1630A>G | ENSP00000514622.1:p.Ile544Val | |
| ENST00000699822.1:c.*1487A>G | ENSP00000514623.1:n.*1487A>G | |
| ENST00000699823.1:c.1630A>G | ENSP00000514624.1:p.Ile544Val | |
| ENST00000699824.1:c.*1538A>G | ENSP00000514625.1:n.*1538A>G | |
| ENST00000699825.1:c.1474A>G | ENSP00000514626.1:p.Ile492Val | |
| ENST00000699826.1:c.*1434A>G | ENSP00000514627.1:n.*1434A>G | |
| ENST00000699827.1:c.1867A>G | ENSP00000514628.1:p.Ile623Val | |
| ENST00000699828.1:c.*1125A>G | ENSP00000514629.1:n.*1125A>G | |
| ENST00000699833.1:n.3807A>G | ||
| ENST00000699837.1:c.1630A>G | ENSP00000514635.1:p.Ile544Val | |
| ENST00000699838.1:c.*1935A>G | ENSP00000514636.1:n.*1935A>G | |
| ENST00000699839.1:c.2221A>G | ENSP00000514637.1:p.Ile741Val | |
| ENST00000699916.1:c.*1292A>G | ENSP00000514684.1:n.*1292A>G | |
| ENST00000699917.1:c.*1484A>G | ENSP00000514685.1:n.*1484A>G | |
| ENST00000699918.1:c.*1536A>G | ENSP00000514686.1:n.*1536A>G | |
| ENST00000699919.1:c.*1622A>G | ENSP00000514687.1:n.*1622A>G | |
| ENST00000699920.1:c.*1671A>G | ENSP00000514688.1:n.*1671A>G | |
| ENST00000699928.1:c.1017A>G | ENSP00000514693.1:p.Ser339= | |
| ENST00000699951.1:c.*1131A>G | ENSP00000514706.1:n.*1131A>G | |
| ENST00000699952.1:c.804-9421A>G | ENSP00000514707.1:n.804-9421A>G | |
| ENST00000265849.12:c.2035A>G MANE Select | ENSP00000265849.7:p.Ile679Val | |
| ENST00000642292.1:c.1630A>G | ENSP00000495524.1:p.Ile544Val | |
| ENST00000642456.1:c.1630A>G | ENSP00000493814.1:p.Ile544Val | |
| ENST00000643595.1:c.*1434A>G | ENSP00000494497.1:n.*1434A>G | |
| ENST00000644110.1:c.1717A>G | ENSP00000496392.1:p.Ile573Val | |
| ENST00000265849.11:c.2035A>G | ENSP00000265849.7:p.Ile679Val | |
| ENST00000382321.5:c.832A>G | ENSP00000371758.4:p.Ile278Val | |
| ENST00000406569.7:n.1678+4124A>G | ||
| ENST00000441476.6:c.1717A>G | ENSP00000392843.2:p.Ile573Val | |
| ENST00000469652.1:n.63-58A>G | ||
| NM_000535.5:c.2035A>G , LRG_161t1:c.2035A>G | NP_000526.1:p.Ile679Val | |
| NR_003085.2:n.2117A>G | ||
| XM_006715742.2:c.2029A>G | XP_006715805.1:p.Ile677Val | |
| XM_006715744.2:c.1102A>G | XP_006715807.1:p.Ile368Val | |
| XM_011515427.1:c.2080A>G | XP_011513729.1:p.Ile694Val | |
| XM_011515428.1:c.1924A>G | XP_011513730.1:p.Ile642Val | |
| XM_011515429.1:c.1717A>G | XP_011513731.1:p.Ile573Val | |
| XM_011515430.1:c.1717A>G | XP_011513732.1:p.Ile573Val | |
| NM_000535.6:c.2035A>G | NP_000526.2:p.Ile679Val | |
| NM_001322003.1:c.1630A>G | NP_001308932.1:p.Ile544Val | |
| NM_001322004.1:c.1630A>G | NP_001308933.1:p.Ile544Val | |
| NM_001322005.1:c.1630A>G | NP_001308934.1:p.Ile544Val | |
| NM_001322006.1:c.1879A>G | NP_001308935.1:p.Ile627Val | |
| NM_001322007.1:c.1717A>G | NP_001308936.1:p.Ile573Val | |
| NM_001322008.1:c.1717A>G | NP_001308937.1:p.Ile573Val | |
| NM_001322009.1:c.1630A>G | NP_001308938.1:p.Ile544Val | |
| NM_001322010.1:c.1474A>G | NP_001308939.1:p.Ile492Val | |
| NM_001322011.1:c.1102A>G | NP_001308940.1:p.Ile368Val | |
| NM_001322012.1:c.1102A>G | NP_001308941.1:p.Ile368Val | |
| NM_001322013.1:c.1462A>G | NP_001308942.1:p.Ile488Val | |
| NM_001322014.1:c.2035A>G | NP_001308943.1:p.Ile679Val | |
| NM_001322015.1:c.1726A>G | NP_001308944.1:p.Ile576Val | |
| NR_136154.1:n.2122A>G | ||
| XM_006715744.4:c.1102A>G | XP_006715807.1:p.Ile368Val | |
| XM_017012342.2:c.1102A>G | XP_016867831.1:p.Ile368Val | |
| XM_024446800.1:c.1474A>G | XP_024302568.1:p.Ile492Val | |
| NM_000535.7:c.2035A>G MANE Select | NP_000526.2:p.Ile679Val | |
| NM_001322003.2:c.1630A>G | NP_001308932.1:p.Ile544Val | |
| NM_001322004.2:c.1630A>G | NP_001308933.1:p.Ile544Val | |
| NM_001322005.2:c.1630A>G | NP_001308934.1:p.Ile544Val | |
| NM_001322006.2:c.1879A>G | NP_001308935.1:p.Ile627Val | |
| NM_001322008.2:c.1717A>G | NP_001308937.1:p.Ile573Val | |
| NM_001322009.2:c.1630A>G | NP_001308938.1:p.Ile544Val | |
| NM_001322010.2:c.1474A>G | NP_001308939.1:p.Ile492Val | |
| NM_001322011.2:c.1102A>G | NP_001308940.1:p.Ile368Val | |
| NM_001322012.2:c.1102A>G | NP_001308941.1:p.Ile368Val | |
| NM_001322013.2:c.1462A>G | NP_001308942.1:p.Ile488Val | |
| NM_001322014.2:c.2035A>G | NP_001308943.1:p.Ile679Val | |
| NM_001322015.2:c.1726A>G | NP_001308944.1:p.Ile576Val | |
| NM_001322007.2:c.1717A>G | NP_001308936.1:p.Ile573Val |