Linked Data
ClinVar Variation Id:
525783
dbSNP Id:
rs372172981
ExAC:
7:6031663 T / C
gnomAD v2:
7-6031663-T-C
gnomAD v4:
7-5992032-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5992032T>C , CM000669.2:g.5992032T>C | GRCh38 |
| NC_000007.13:g.6031663T>C , CM000669.1:g.6031663T>C | GRCh37 |
| NC_000007.12:g.5998189T>C | NCBI36 |
| NG_008466.1:g.22075A>G , LRG_161:g.22075A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699814.2:c.*325A>G | ENSP00000514615.2:n.*325A>G | |
| ENST00000699840.2:c.926A>G | ENSP00000514638.2:p.Tyr309Cys | |
| ENST00000699930.2:c.821A>G | ENSP00000514695.2:p.Tyr274Cys | |
| ENST00000406569.8:c.929A>G | ENSP00000514464.1:p.Tyr310Cys | |
| ENST00000644110.2:c.*523A>G | ENSP00000496392.2:n.*523A>G | |
| ENST00000699752.1:c.929A>G | ENSP00000514561.1:p.Tyr310Cys | |
| ENST00000699753.1:c.*228A>G | ENSP00000514562.1:n.*228A>G | |
| ENST00000699754.1:c.731A>G | ENSP00000514563.1:p.Tyr244Cys | |
| ENST00000699755.1:c.*328A>G | ENSP00000514564.1:n.*328A>G | |
| ENST00000699756.1:c.*516A>G | ENSP00000514565.1:n.*516A>G | |
| ENST00000699757.1:c.*186A>G | ENSP00000514566.1:n.*186A>G | |
| ENST00000699758.1:c.*186A>G | ENSP00000514567.1:n.*186A>G | |
| ENST00000699759.1:n.1783A>G | ||
| ENST00000699760.1:c.611A>G | ENSP00000514568.1:p.Tyr204Cys | |
| ENST00000699761.1:c.524A>G | ENSP00000514569.1:p.Tyr175Cys | |
| ENST00000699762.1:c.356A>G | ENSP00000514570.1:p.Tyr119Cys | |
| ENST00000699763.1:c.524A>G | ENSP00000514571.1:p.Tyr175Cys | |
| ENST00000699764.1:c.929A>G | ENSP00000514572.1:p.Tyr310Cys | |
| ENST00000699765.1:c.*25A>G | ENSP00000514573.1:n.*25A>G | |
| ENST00000699766.1:c.929A>G | ENSP00000514574.1:p.Tyr310Cys | |
| ENST00000699767.1:c.929A>G | ENSP00000514575.1:p.Tyr310Cys | |
| ENST00000699768.1:c.929A>G | ENSP00000514576.1:p.Tyr310Cys | |
| ENST00000699811.1:c.524A>G | ENSP00000514614.1:p.Tyr175Cys | |
| ENST00000699813.1:n.1042A>G | ||
| ENST00000699814.1:c.552A>G | ||
| ENST00000699815.1:c.*421A>G | ENSP00000514616.1:n.*421A>G | |
| ENST00000699816.1:c.524A>G | ENSP00000514617.1:p.Tyr175Cys | |
| ENST00000699817.1:c.*523A>G | ENSP00000514618.1:n.*523A>G | |
| ENST00000699818.1:c.524A>G | ENSP00000514619.1:p.Tyr175Cys | |
| ENST00000699819.1:c.*86A>G | ENSP00000514620.1:n.*86A>G | |
| ENST00000699820.1:c.929A>G | ENSP00000514621.1:p.Tyr310Cys | |
| ENST00000699821.1:c.524A>G | ENSP00000514622.1:p.Tyr175Cys | |
| ENST00000699822.1:c.*381A>G | ENSP00000514623.1:n.*381A>G | |
| ENST00000699823.1:c.524A>G | ENSP00000514624.1:p.Tyr175Cys | |
| ENST00000699824.1:c.*432A>G | ENSP00000514625.1:n.*432A>G | |
| ENST00000699825.1:c.524A>G | ENSP00000514626.1:p.Tyr175Cys | |
| ENST00000699826.1:c.*328A>G | ENSP00000514627.1:n.*328A>G | |
| ENST00000699827.1:c.761A>G | ENSP00000514628.1:p.Tyr254Cys | |
| ENST00000699828.1:c.929A>G | ENSP00000514629.1:p.Tyr310Cys | |
| ENST00000699829.1:c.*430A>G | ENSP00000514630.1:n.*430A>G | |
| ENST00000699830.1:c.*328A>G | ENSP00000514631.1:n.*328A>G | |
| ENST00000699833.1:n.2701A>G | ||
| ENST00000699837.1:c.524A>G | ENSP00000514635.1:p.Tyr175Cys | |
| ENST00000699838.1:c.*829A>G | ENSP00000514636.1:n.*829A>G | |
| ENST00000699839.1:c.1115A>G | ENSP00000514637.1:p.Tyr372Cys | |
| ENST00000699840.1:c.926A>G | ENSP00000514638.1:p.Tyr309Cys | |
| ENST00000699916.1:c.*186A>G | ENSP00000514684.1:n.*186A>G | |
| ENST00000699917.1:c.*378A>G | ENSP00000514685.1:n.*378A>G | |
| ENST00000699918.1:c.*430A>G | ENSP00000514686.1:n.*430A>G | |
| ENST00000699919.1:c.*516A>G | ENSP00000514687.1:n.*516A>G | |
| ENST00000699920.1:c.*565A>G | ENSP00000514688.1:n.*565A>G | |
| ENST00000699928.1:c.929A>G | ENSP00000514693.1:p.Tyr310Cys | |
| ENST00000699929.1:c.*230A>G | ENSP00000514694.1:n.*230A>G | |
| ENST00000699930.1:c.821A>G | ENSP00000514695.1:p.Tyr274Cys | |
| ENST00000699931.1:n.2357A>G | ||
| ENST00000699932.1:c.*25A>G | ENSP00000514696.1:n.*25A>G | |
| ENST00000699933.1:n.909A>G | ||
| ENST00000699951.1:c.*25A>G | ENSP00000514706.1:n.*25A>G | |
| ENST00000699952.1:c.803+5294A>G | ENSP00000514707.1:n.803+5294A>G | |
| ENST00000699953.1:c.*36A>G | ENSP00000514708.1:n.*36A>G | |
| ENST00000699954.1:c.*230A>G | ENSP00000514709.1:n.*230A>G | |
| ENST00000265849.12:c.929A>G MANE Select | ENSP00000265849.7:p.Tyr310Cys | |
| ENST00000642292.1:c.524A>G | ENSP00000495524.1:p.Tyr175Cys | |
| ENST00000642456.1:c.524A>G | ENSP00000493814.1:p.Tyr175Cys | |
| ENST00000643595.1:c.*328A>G | ENSP00000494497.1:n.*328A>G | |
| ENST00000644110.1:c.611A>G | ENSP00000496392.1:p.Tyr204Cys | |
| ENST00000265849.11:c.929A>G | ENSP00000265849.7:p.Tyr310Cys | |
| ENST00000382321.5:c.803+5294A>G | ENSP00000371758.4:n.803+5294A>G | |
| ENST00000406569.7:n.929A>G | ||
| ENST00000441476.6:c.611A>G | ENSP00000392843.2:p.Tyr204Cys | |
| ENST00000469652.1:n.63-9127A>G | ||
| NM_000535.5:c.929A>G , LRG_161t1:c.929A>G | NP_000526.1:p.Tyr310Cys | |
| NR_003085.2:n.1011A>G | ||
| XM_006715742.2:c.923A>G | XP_006715805.1:p.Tyr308Cys | |
| XM_006715744.2:c.-5A>G | XP_006715807.1:n.-5A>G | |
| XM_011515427.1:c.974A>G | XP_011513729.1:p.Tyr325Cys | |
| XM_011515428.1:c.974A>G | XP_011513730.1:p.Tyr325Cys | |
| XM_011515429.1:c.611A>G | XP_011513731.1:p.Tyr204Cys | |
| XM_011515430.1:c.611A>G | XP_011513732.1:p.Tyr204Cys | |
| NM_000535.6:c.929A>G | NP_000526.2:p.Tyr310Cys | |
| NM_001322003.1:c.524A>G | NP_001308932.1:p.Tyr175Cys | |
| NM_001322004.1:c.524A>G | NP_001308933.1:p.Tyr175Cys | |
| NM_001322005.1:c.524A>G | NP_001308934.1:p.Tyr175Cys | |
| NM_001322006.1:c.929A>G | NP_001308935.1:p.Tyr310Cys | |
| NM_001322007.1:c.611A>G | NP_001308936.1:p.Tyr204Cys | |
| NM_001322008.1:c.611A>G | NP_001308937.1:p.Tyr204Cys | |
| NM_001322009.1:c.524A>G | NP_001308938.1:p.Tyr175Cys | |
| NM_001322010.1:c.524A>G | NP_001308939.1:p.Tyr175Cys | |
| NM_001322011.1:c.-5A>G | NP_001308940.1:n.-5A>G | |
| NM_001322012.1:c.-5A>G | NP_001308941.1:n.-5A>G | |
| NM_001322013.1:c.356A>G | NP_001308942.1:p.Tyr119Cys | |
| NM_001322014.1:c.929A>G | NP_001308943.1:p.Tyr310Cys | |
| NM_001322015.1:c.620A>G | NP_001308944.1:p.Tyr207Cys | |
| NR_136154.1:n.1016A>G | ||
| XM_006715744.4:c.-5A>G | XP_006715807.1:n.-5A>G | |
| XM_017012342.2:c.-5A>G | XP_016867831.1:n.-5A>G | |
| XM_024446800.1:c.524A>G | XP_024302568.1:p.Tyr175Cys | |
| NM_000535.7:c.929A>G MANE Select | NP_000526.2:p.Tyr310Cys | |
| NM_001322003.2:c.524A>G | NP_001308932.1:p.Tyr175Cys | |
| NM_001322004.2:c.524A>G | NP_001308933.1:p.Tyr175Cys | |
| NM_001322005.2:c.524A>G | NP_001308934.1:p.Tyr175Cys | |
| NM_001322006.2:c.929A>G | NP_001308935.1:p.Tyr310Cys | |
| NM_001322008.2:c.611A>G | NP_001308937.1:p.Tyr204Cys | |
| NM_001322009.2:c.524A>G | NP_001308938.1:p.Tyr175Cys | |
| NM_001322010.2:c.524A>G | NP_001308939.1:p.Tyr175Cys | |
| NM_001322011.2:c.-5A>G | NP_001308940.1:n.-5A>G | |
| NM_001322012.2:c.-5A>G | NP_001308941.1:n.-5A>G | |
| NM_001322013.2:c.356A>G | NP_001308942.1:p.Tyr119Cys | |
| NM_001322014.2:c.929A>G | NP_001308943.1:p.Tyr310Cys | |
| NM_001322015.2:c.620A>G | NP_001308944.1:p.Tyr207Cys | |
| NM_001322007.2:c.611A>G | NP_001308936.1:p.Tyr204Cys |