Linked Data
ClinVar Variation Id:
195780
dbSNP Id:
rs146818399
ExAC:
3:129225350 T / G
gnomAD v2:
3-129225350-T-G
gnomAD v3:
3-129506507-T-G
gnomAD v4:
3-129506507-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129506507T>G , CM000665.2:g.129506507T>G | GRCh38 |
| NC_000003.11:g.129225350T>G , CM000665.1:g.129225350T>G | GRCh37 |
| NC_000003.10:g.130708040T>G | NCBI36 |
| NG_023392.1:g.71383T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000431818.8:c.*2008T>G | ENSP00000410946.3:n.*2008T>G | |
| ENST00000440957.7:c.*2070T>G | ENSP00000401569.3:n.*2070T>G | |
| ENST00000504021.6:c.2362T>G | ENSP00000422179.2:p.Tyr788Asp | |
| ENST00000504444.2:n.759T>G | ||
| ENST00000507221.2:c.835T>G | ENSP00000427515.2:p.Tyr279Asp | |
| ENST00000513932.2:n.1039T>G | ||
| ENST00000515783.6:c.2254T>G | ENSP00000423288.2:p.Tyr752Asp | |
| ENST00000685087.1:c.2305T>G | ENSP00000509245.1:p.Tyr769Asp | |
| ENST00000685122.1:c.835T>G | ENSP00000510278.1:p.Tyr279Asp | |
| ENST00000685189.1:c.*2480T>G | ENSP00000510418.1:n.*2480T>G | |
| ENST00000685282.1:c.2646T>G | ENSP00000508642.1:p.Ile882Met | |
| ENST00000685447.1:c.2415T>G | ENSP00000509155.1:p.Ile805Met | |
| ENST00000685512.1:n.3345T>G | ||
| ENST00000685621.1:n.1216T>G | ||
| ENST00000685811.1:n.3487T>G | ||
| ENST00000685921.1:c.2461T>G | ENSP00000509914.1:p.Tyr821Asp | |
| ENST00000685939.1:c.*1169T>G | ENSP00000509414.1:n.*1169T>G | |
| ENST00000686375.1:c.*1169T>G | ENSP00000510777.1:n.*1169T>G | |
| ENST00000686473.1:c.2407T>G | ENSP00000508526.1:p.Tyr803Asp | |
| ENST00000686531.1:c.2353T>G | ENSP00000510570.1:p.Tyr785Asp | |
| ENST00000686614.1:n.1296T>G | ||
| ENST00000686830.1:c.2410T>G | ENSP00000510002.1:p.Tyr804Asp | |
| ENST00000687377.1:c.2695T>G | ENSP00000509225.1:p.Tyr899Asp | |
| ENST00000687398.1:c.*2207T>G | ENSP00000510191.1:n.*2207T>G | |
| ENST00000687461.1:n.3111T>G | ||
| ENST00000687645.1:c.2749T>G | ENSP00000510672.1:p.Tyr917Asp | |
| ENST00000687766.1:c.*341T>G | ENSP00000509886.1:n.*341T>G | |
| ENST00000687791.1:c.2518T>G | ENSP00000509224.1:p.Tyr840Asp | |
| ENST00000687845.1:c.2259T>G | ENSP00000508687.1:p.Ile753Met | |
| ENST00000687864.1:n.2769T>G | ||
| ENST00000688020.1:c.2593T>G | ENSP00000508904.1:p.Tyr865Asp | |
| ENST00000688129.1:c.*2351T>G | ENSP00000509382.1:n.*2351T>G | |
| ENST00000688266.1:n.2357T>G | ||
| ENST00000688392.1:n.3160T>G | ||
| ENST00000688504.1:n.2715T>G | ||
| ENST00000688527.1:c.889T>G | ENSP00000508740.1:p.Tyr297Asp | |
| ENST00000688657.1:c.727T>G | ENSP00000508933.1:p.Tyr243Asp | |
| ENST00000688664.1:c.*1997T>G | ENSP00000510359.1:n.*1997T>G | |
| ENST00000688970.1:n.2953T>G | ||
| ENST00000689005.1:c.2269T>G | ENSP00000510168.1:p.Tyr757Asp | |
| ENST00000689313.1:c.2725T>G | ENSP00000509012.1:p.Tyr909Asp | |
| ENST00000689332.1:c.2572T>G | ENSP00000510425.1:p.Tyr858Asp | |
| ENST00000689384.1:n.3316T>G | ||
| ENST00000689492.1:c.2425T>G | ENSP00000510239.1:p.Tyr809Asp | |
| ENST00000689643.1:c.2749T>G | ENSP00000509801.1:p.Tyr917Asp | |
| ENST00000689796.1:c.2410T>G | ENSP00000509716.1:p.Tyr804Asp | |
| ENST00000689801.1:c.2518T>G | ENSP00000509982.1:p.Tyr840Asp | |
| ENST00000689871.1:c.2518T>G | ENSP00000510412.1:p.Tyr840Asp | |
| ENST00000689884.1:n.1733T>G | ||
| ENST00000690209.1:c.2572T>G | ENSP00000509005.1:p.Tyr858Asp | |
| ENST00000690617.1:n.2686T>G | ||
| ENST00000690657.1:c.889T>G | ENSP00000510699.1:p.Tyr297Asp | |
| ENST00000690663.1:c.2362T>G | ENSP00000509297.1:p.Tyr788Asp | |
| ENST00000690677.1:c.*1909T>G | ENSP00000510036.1:n.*1909T>G | |
| ENST00000690723.1:c.2572T>G | ENSP00000508811.1:p.Tyr858Asp | |
| ENST00000690862.1:c.2518T>G | ENSP00000509210.1:p.Tyr840Asp | |
| ENST00000691148.1:n.3216T>G | ||
| ENST00000691360.1:c.*2175T>G | ENSP00000510040.1:n.*2175T>G | |
| ENST00000691583.1:c.2518T>G | ENSP00000510741.1:p.Tyr840Asp | |
| ENST00000691641.1:c.*2297T>G | ENSP00000509350.1:n.*2297T>G | |
| ENST00000691705.1:c.2572T>G | ENSP00000510077.1:p.Tyr858Asp | |
| ENST00000691733.1:c.2572T>G | ENSP00000509735.1:p.Tyr858Asp | |
| ENST00000691770.1:c.*101T>G | ENSP00000510126.1:n.*101T>G | |
| ENST00000691964.1:c.2518T>G | ENSP00000509094.1:p.Tyr840Asp | |
| ENST00000692228.1:c.*1646T>G | ENSP00000508464.1:n.*1646T>G | |
| ENST00000692242.1:c.2749T>G | ENSP00000509878.1:p.Tyr917Asp | |
| ENST00000692321.1:c.2068T>G | ENSP00000508614.1:p.Tyr690Asp | |
| ENST00000692391.1:c.2572T>G | ENSP00000509211.1:p.Tyr858Asp | |
| ENST00000692508.1:n.3396T>G | ||
| ENST00000692728.1:c.2068T>G | ENSP00000510105.1:p.Tyr690Asp | |
| ENST00000692901.1:c.2341T>G | ENSP00000510339.1:p.Tyr781Asp | |
| ENST00000692929.1:n.1603T>G | ||
| ENST00000692985.1:c.*2384T>G | ENSP00000510460.1:n.*2384T>G | |
| ENST00000693114.1:c.*1583T>G | ENSP00000508738.1:n.*1583T>G | |
| ENST00000693129.1:c.2695T>G | ENSP00000509806.1:p.Tyr899Asp | |
| ENST00000693162.1:c.2572T>G | ENSP00000509103.1:p.Tyr858Asp | |
| ENST00000693233.1:c.2122T>G | ENSP00000509186.1:p.Tyr708Asp | |
| ENST00000693489.1:c.2686T>G | ENSP00000509656.1:p.Tyr896Asp | |
| ENST00000693588.1:c.2416T>G | ENSP00000509216.1:p.Tyr806Asp | |
| ENST00000693654.1:n.2986T>G | ||
| ENST00000348417.7:c.2749T>G MANE Select | ENSP00000324005.4:p.Tyr917Asp | |
| ENST00000296266.7:c.2902T>G | ENSP00000296266.3:p.Tyr968Asp | |
| ENST00000347300.6:c.2572T>G | ENSP00000323973.3:p.Tyr858Asp | |
| ENST00000348417.6:c.2749T>G | ENSP00000324005.3:p.Tyr917Asp | |
| ENST00000349441.6:c.2416T>G | ENSP00000324165.3:p.Tyr806Asp | |
| ENST00000431818.6:c.2299T>G | ENSP00000410946.2:p.Tyr767Asp | |
| ENST00000440957.6:c.2122T>G | ENSP00000401569.2:p.Tyr708Asp | |
| ENST00000504021.5:c.2377T>G | ENSP00000422179.1:p.Tyr793Asp | |
| ENST00000506507.5:n.2532T>G | ||
| ENST00000507564.5:c.2725T>G | ENSP00000425536.1:p.Tyr909Asp | |
| ENST00000511425.5:n.1158T>G | ||
| ENST00000512220.5:c.*2657T>G | ENSP00000421953.1:n.*2657T>G | |
| NM_001280541.1:c.2725T>G | NP_001267470.1:p.Tyr909Asp | |
| NM_001280545.1:c.2299T>G | NP_001267474.1:p.Tyr767Asp | |
| NM_001280546.1:c.2122T>G | NP_001267475.1:p.Tyr708Asp | |
| NM_018262.3:c.2572T>G | NP_060732.2:p.Tyr858Asp | |
| NM_052985.3:c.2902T>G | NP_443711.2:p.Tyr968Asp | |
| NM_052989.2:c.2749T>G | NP_443715.1:p.Tyr917Asp | |
| NM_052990.2:c.2416T>G | NP_443716.1:p.Tyr806Asp | |
| XM_005247609.1:c.2572T>G | XP_005247666.1:p.Tyr858Asp | |
| XM_006713689.1:c.2749T>G | XP_006713752.1:p.Tyr917Asp | |
| XM_006713691.2:c.2695T>G | XP_006713754.1:p.Tyr899Asp | |
| XM_006713692.2:c.2518T>G | XP_006713755.1:p.Tyr840Asp | |
| XM_011512967.1:c.2593T>G | XP_011511269.1:p.Tyr865Asp | |
| XM_011512968.1:c.2299T>G | XP_011511270.1:p.Tyr767Asp | |
| XM_011512969.1:c.2299T>G | XP_011511271.1:p.Tyr767Asp | |
| XM_011512970.1:c.2299T>G | XP_011511272.1:p.Tyr767Asp | |
| XM_011512971.1:c.2122T>G | XP_011511273.1:p.Tyr708Asp | |
| XM_011512972.1:c.2749T>G | XP_011511274.1:p.Tyr917Asp | |
| XM_011512973.1:c.1345T>G | XP_011511275.1:p.Tyr449Asp | |
| XM_005247609.2:c.2572T>G | XP_005247666.1:p.Tyr858Asp | |
| XM_006713689.2:c.2749T>G | XP_006713752.1:p.Tyr917Asp | |
| XM_006713691.3:c.2695T>G | XP_006713754.1:p.Tyr899Asp | |
| XM_006713692.3:c.2518T>G | XP_006713755.1:p.Tyr840Asp | |
| XM_011512972.3:c.2749T>G | XP_011511274.1:p.Tyr917Asp | |
| XM_017006817.2:c.2749T>G | XP_016862306.1:p.Tyr917Asp | |
| XM_017006818.2:c.2749T>G | XP_016862307.1:p.Tyr917Asp | |
| XM_017006819.2:c.2695T>G | XP_016862308.1:p.Tyr899Asp | |
| XM_017006820.2:c.2695T>G | XP_016862309.1:p.Tyr899Asp | |
| XM_017006821.2:c.2695T>G | XP_016862310.1:p.Tyr899Asp | |
| XM_017006822.2:c.2593T>G | XP_016862311.1:p.Tyr865Asp | |
| XM_017006823.2:c.2572T>G | XP_016862312.1:p.Tyr858Asp | |
| XM_017006824.2:c.2572T>G | XP_016862313.1:p.Tyr858Asp | |
| XM_017006825.2:c.2518T>G | XP_016862314.1:p.Tyr840Asp | |
| XM_017006826.2:c.2518T>G | XP_016862315.1:p.Tyr840Asp | |
| XM_017006827.2:c.2518T>G | XP_016862316.1:p.Tyr840Asp | |
| XM_017006828.2:c.2416T>G | XP_016862317.1:p.Tyr806Asp | |
| XM_017006829.2:c.2416T>G | XP_016862318.1:p.Tyr806Asp | |
| XM_017006830.2:c.2299T>G | XP_016862319.1:p.Tyr767Asp | |
| XM_017006831.1:c.2299T>G | XP_016862320.1:p.Tyr767Asp | |
| XM_017006832.1:c.2299T>G | XP_016862321.1:p.Tyr767Asp | |
| XM_017006833.2:c.2362T>G | XP_016862322.1:p.Tyr788Asp | |
| XM_017006834.2:c.2362T>G | XP_016862323.1:p.Tyr788Asp | |
| XM_017006835.1:c.2122T>G | XP_016862324.1:p.Tyr708Asp | |
| XM_017006836.2:c.2068T>G | XP_016862325.1:p.Tyr690Asp | |
| XM_017006837.1:c.1345T>G | XP_016862326.1:p.Tyr449Asp | |
| XM_017006838.2:c.1345T>G | XP_016862327.1:p.Tyr449Asp | |
| XM_024453639.1:c.1792T>G | XP_024309407.1:p.Tyr598Asp | |
| NM_001280541.2:c.2725T>G | NP_001267470.1:p.Tyr909Asp | |
| NM_018262.4:c.2572T>G | NP_060732.2:p.Tyr858Asp | |
| NM_052985.4:c.2902T>G | NP_443711.2:p.Tyr968Asp | |
| NM_052989.3:c.2749T>G MANE Select | NP_443715.1:p.Tyr917Asp | |
| NM_052990.3:c.2416T>G | NP_443716.1:p.Tyr806Asp | |
| NM_001280545.2:c.2299T>G | NP_001267474.1:p.Tyr767Asp | |
| NM_001280546.2:c.2122T>G | NP_001267475.1:p.Tyr708Asp |