Linked Data
ClinVar Variation Id:
94449
dbSNP Id:
rs398123848
ExAC:
X:31164403 C / T
gnomAD v2:
X-31164403-C-T
gnomAD v3:
X-31146286-C-T
gnomAD v4:
X-31146286-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31146286C>T , CM000685.2:g.31146286C>T | GRCh38 |
| NC_000023.10:g.31164403C>T , CM000685.1:g.31164403C>T | GRCh37 |
| NC_000023.9:g.31074324C>T | NCBI36 |
| NG_012232.1:g.2198324G>A , LRG_199:g.2198324G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.5728+5G>A | ENSP00000350765.3:n.5728+5G>A | |
| ENST00000680162.2:c.1612+5G>A | ENSP00000506634.2:n.1612+5G>A | |
| ENST00000680768.2:c.1618+5G>A | ENSP00000506359.2:n.1618+5G>A | |
| ENST00000681989.1:n.1719+5G>A | ||
| ENST00000682207.1:n.1041+5G>A | ||
| ENST00000682238.1:c.3211+5G>A | ENSP00000508124.1:n.3211+5G>A | |
| ENST00000682322.1:c.1612+5G>A | ENSP00000507690.1:n.1612+5G>A | |
| ENST00000682600.1:c.1678+5G>A | ENSP00000507640.1:n.1678+5G>A | |
| ENST00000682746.1:n.311+5G>A | ||
| ENST00000682769.1:n.1513+5G>A | ||
| ENST00000683503.1:n.2736+5G>A | ||
| ENST00000683509.1:n.2399+5G>A | ||
| ENST00000683675.1:n.2020+5G>A | ||
| ENST00000683709.1:n.2400+5G>A | ||
| ENST00000683995.1:n.1066+5G>A | ||
| ENST00000684072.1:n.1150+5G>A | ||
| ENST00000684103.1:n.1329+5G>A | ||
| ENST00000684130.1:c.3502+5G>A | ENSP00000508037.1:n.3502+5G>A | |
| ENST00000684247.1:n.393+5G>A | ||
| ENST00000684342.1:n.1965+5G>A | ||
| ENST00000684350.1:n.2736+5G>A | ||
| ENST00000343523.7:c.2776+5G>A | ENSP00000340057.4:n.2776+5G>A | |
| ENST00000357033.9:c.10921+5G>A MANE Select | ENSP00000354923.3:n.10921+5G>A | |
| ENST00000619831.5:c.6889+5G>A | ENSP00000479270.2:n.6889+5G>A | |
| ENST00000620040.5:c.3335+1032G>A | ENSP00000478150.2:n.3335+1032G>A | |
| ENST00000679437.1:c.583+5G>A | ENSP00000506629.1:n.583+5G>A | |
| ENST00000679641.1:c.*593+5G>A | ENSP00000506135.1:n.*593+5G>A | |
| ENST00000679706.1:c.548+5G>A | ||
| ENST00000679850.1:n.5932+5G>A | ||
| ENST00000680162.1:c.1594+5G>A | ENSP00000506634.1:n.1594+5G>A | |
| ENST00000680355.1:c.1387+5G>A | ENSP00000506257.1:n.1387+5G>A | |
| ENST00000680557.1:c.604-12092G>A | ENSP00000505164.1:n.604-12092G>A | |
| ENST00000680701.1:n.696+5G>A | ||
| ENST00000680768.1:c.1621+5G>A | ENSP00000506359.1:n.1621+5G>A | |
| ENST00000680961.1:c.*884+5G>A | ENSP00000506386.1:n.*884+5G>A | |
| ENST00000681026.1:c.583+5G>A | ENSP00000506689.1:n.583+5G>A | |
| ENST00000681153.1:c.1678+5G>A | ENSP00000505124.1:n.1678+5G>A | |
| ENST00000343523.6:c.2734+5G>A | ENSP00000340057.3:n.2734+5G>A | |
| ENST00000357033.8:c.10921+5G>A | ENSP00000354923.3:n.10921+5G>A | |
| ENST00000358062.6:c.3970+5G>A | ENSP00000350765.2:n.3970+5G>A | |
| ENST00000359836.5:c.3502+5G>A | ENSP00000352894.1:n.3502+5G>A | |
| ENST00000361471.8:c.1678+5G>A | ENSP00000354464.4:n.1678+5G>A | |
| ENST00000378677.6:c.10909+5G>A | ENSP00000367948.2:n.10909+5G>A | |
| ENST00000378680.6:c.1387+5G>A | ENSP00000367951.2:n.1387+5G>A | |
| ENST00000378702.8:c.1717+5G>A | ENSP00000367974.4:n.1717+5G>A | |
| ENST00000378707.7:c.3541+5G>A | ENSP00000367979.3:n.3541+5G>A | |
| ENST00000378723.7:c.1717+5G>A | ENSP00000367997.3:n.1717+5G>A | |
| ENST00000474231.5:c.3541+5G>A | ENSP00000417123.1:n.3541+5G>A | |
| ENST00000481143.2:n.114+23157G>A | ||
| ENST00000541735.5:c.3211+5G>A | ENSP00000444119.1:n.3211+5G>A | |
| ENST00000619831.4:c.10906+5G>A | ENSP00000479270.1:n.10906+5G>A | |
| ENST00000620040.4:c.10918+5G>A | ENSP00000478150.1:n.10918+5G>A | |
| NM_000109.3:c.10897+5G>A | NP_000100.2:n.10897+5G>A | |
| NM_004006.2:c.10921+5G>A , LRG_199t1:c.10921+5G>A | NP_003997.1:n.10921+5G>A | |
| NM_004009.3:c.10909+5G>A | NP_004000.1:n.10909+5G>A | |
| NM_004010.3:c.10552+5G>A | NP_004001.1:n.10552+5G>A | |
| NM_004011.3:c.6898+5G>A | NP_004002.2:n.6898+5G>A | |
| NM_004012.3:c.6889+5G>A | NP_004003.1:n.6889+5G>A | |
| NM_004013.2:c.3541+5G>A | NP_004004.1:n.3541+5G>A | |
| NM_004014.2:c.2734+5G>A | NP_004005.1:n.2734+5G>A | |
| NM_004015.2:c.1717+5G>A | NP_004006.1:n.1717+5G>A | |
| NM_004016.2:c.1717+5G>A | NP_004007.1:n.1717+5G>A | |
| NM_004017.2:c.1678+5G>A | NP_004008.1:n.1678+5G>A | |
| NM_004018.2:c.1678+5G>A | NP_004009.1:n.1678+5G>A | |
| NM_004020.3:c.3211+5G>A | NP_004011.2:n.3211+5G>A | |
| NM_004021.2:c.3541+5G>A | NP_004012.1:n.3541+5G>A | |
| NM_004022.2:c.3502+5G>A | NP_004013.1:n.3502+5G>A | |
| NM_004023.2:c.3211+5G>A | NP_004014.1:n.3211+5G>A | |
| XM_006724468.2:c.10921+5G>A | XP_006724531.1:n.10921+5G>A | |
| XM_006724469.2:c.10897+5G>A | XP_006724532.1:n.10897+5G>A | |
| XM_006724470.2:c.10882+5G>A | XP_006724533.1:n.10882+5G>A | |
| XM_006724471.2:c.10816+5G>A | XP_006724534.1:n.10816+5G>A | |
| XM_006724472.2:c.10792+5G>A | XP_006724535.1:n.10792+5G>A | |
| XM_006724473.2:c.10783+5G>A | XP_006724536.1:n.10783+5G>A | |
| XM_006724474.2:c.10591+5G>A | XP_006724537.1:n.10591+5G>A | |
| XM_006724475.2:c.10591+5G>A | XP_006724538.1:n.10591+5G>A | |
| XM_011545467.1:c.10798+5G>A | XP_011543769.1:n.10798+5G>A | |
| XM_006724469.3:c.10897+5G>A | XP_006724532.1:n.10897+5G>A | |
| XM_006724470.3:c.10882+5G>A | XP_006724533.1:n.10882+5G>A | |
| XM_006724474.3:c.10591+5G>A | XP_006724537.1:n.10591+5G>A | |
| XM_017029328.1:c.10882+5G>A | XP_016884817.1:n.10882+5G>A | |
| XM_017029331.1:c.5095+5G>A | XP_016884820.1:n.5095+5G>A | |
| NM_000109.4:c.10897+5G>A | NP_000100.3:n.10897+5G>A | |
| NM_004006.3:c.10921+5G>A MANE Select | NP_003997.2:n.10921+5G>A | |
| NM_004011.4:c.6898+5G>A | NP_004002.3:n.6898+5G>A | |
| NM_004012.4:c.6889+5G>A | NP_004003.2:n.6889+5G>A | |
| NM_004015.3:c.1717+5G>A | NP_004006.1:n.1717+5G>A | |
| NM_004016.3:c.1717+5G>A | NP_004007.1:n.1717+5G>A | |
| NM_004017.3:c.1678+5G>A | NP_004008.1:n.1678+5G>A | |
| NM_004018.3:c.1678+5G>A | NP_004009.1:n.1678+5G>A | |
| NM_004021.3:c.3541+5G>A | NP_004012.2:n.3541+5G>A | |
| NM_004023.3:c.3211+5G>A | NP_004014.2:n.3211+5G>A | |
| NM_004013.3:c.3541+5G>A | NP_004004.2:n.3541+5G>A | |
| NM_004014.3:c.2734+5G>A | NP_004005.2:n.2734+5G>A | |
| NM_004020.4:c.3211+5G>A | NP_004011.3:n.3211+5G>A | |
| NM_004022.3:c.3502+5G>A | NP_004013.2:n.3502+5G>A |