Linked Data
ClinVar Variation Id:
239610
dbSNP Id:
rs748786108
ExAC:
X:31854826 C / T
gnomAD v2:
X-31854826-C-T
gnomAD v3:
X-31836709-C-T
gnomAD v4:
X-31836709-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.31836709C>T , CM000685.2:g.31836709C>T | GRCh38 |
| NC_000023.10:g.31854826C>T , CM000685.1:g.31854826C>T | GRCh37 |
| NC_000023.9:g.31764747C>T | NCBI36 |
| NG_012232.1:g.1507901G>A , LRG_199:g.1507901G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.2046+9G>A | ENSP00000350765.3:n.2046+9G>A | |
| ENST00000682238.1:c.-181+9G>A | ENSP00000508124.1:n.-181+9G>A | |
| ENST00000683117.1:n.861+9G>A | ||
| ENST00000683450.1:n.783+9G>A | ||
| ENST00000683851.1:n.861+9G>A | ||
| ENST00000683957.1:n.692+9G>A | ||
| ENST00000684130.1:c.-181+9G>A | ENSP00000508037.1:n.-181+9G>A | |
| ENST00000357033.9:c.7200+9G>A MANE Select | ENSP00000354923.3:n.7200+9G>A | |
| ENST00000619831.5:c.3168+9G>A | ENSP00000479270.2:n.3168+9G>A | |
| ENST00000620040.5:c.-181+9G>A | ENSP00000478150.2:n.-181+9G>A | |
| ENST00000680961.1:c.-181+9G>A | ENSP00000506386.1:n.-181+9G>A | |
| ENST00000681646.1:n.861+9G>A | ||
| ENST00000681839.1:c.189+9G>A | ENSP00000505228.1:n.189+9G>A | |
| ENST00000357033.8:c.7200+9G>A | ENSP00000354923.3:n.7200+9G>A | |
| ENST00000358062.6:c.288+9G>A | ENSP00000350765.2:n.288+9G>A | |
| ENST00000359836.5:c.-181+9G>A | ENSP00000352894.1:n.-181+9G>A | |
| ENST00000378677.6:c.7188+9G>A | ENSP00000367948.2:n.7188+9G>A | |
| ENST00000378707.7:c.-181+9G>A | ENSP00000367979.3:n.-181+9G>A | |
| ENST00000471779.1:c.66+9G>A | ENSP00000417075.1:n.66+9G>A | |
| ENST00000474231.5:c.-181+9G>A | ENSP00000417123.1:n.-181+9G>A | |
| ENST00000541735.5:c.-181+9G>A | ENSP00000444119.1:n.-181+9G>A | |
| ENST00000619831.4:c.7185+9G>A | ENSP00000479270.1:n.7185+9G>A | |
| ENST00000620040.4:c.7197+9G>A | ENSP00000478150.1:n.7197+9G>A | |
| NM_000109.3:c.7176+9G>A | NP_000100.2:n.7176+9G>A | |
| NM_004006.2:c.7200+9G>A , LRG_199t1:c.7200+9G>A | NP_003997.1:n.7200+9G>A | |
| NM_004009.3:c.7188+9G>A | NP_004000.1:n.7188+9G>A | |
| NM_004010.3:c.6831+9G>A | NP_004001.1:n.6831+9G>A | |
| NM_004011.3:c.3177+9G>A | NP_004002.2:n.3177+9G>A | |
| NM_004012.3:c.3168+9G>A | NP_004003.1:n.3168+9G>A | |
| NM_004013.2:c.-181+9G>A | NP_004004.1:n.-181+9G>A | |
| NM_004020.3:c.-181+9G>A | NP_004011.2:n.-181+9G>A | |
| NM_004021.2:c.-181+9G>A | NP_004012.1:n.-181+9G>A | |
| NM_004022.2:c.-181+9G>A | NP_004013.1:n.-181+9G>A | |
| NM_004023.2:c.-181+9G>A | NP_004014.1:n.-181+9G>A | |
| XM_006724468.2:c.7200+9G>A | XP_006724531.1:n.7200+9G>A | |
| XM_006724469.2:c.7176+9G>A | XP_006724532.1:n.7176+9G>A | |
| XM_006724470.2:c.7200+9G>A | XP_006724533.1:n.7200+9G>A | |
| XM_006724471.2:c.7200+9G>A | XP_006724534.1:n.7200+9G>A | |
| XM_006724472.2:c.7071+9G>A | XP_006724535.1:n.7071+9G>A | |
| XM_006724473.2:c.7062+9G>A | XP_006724536.1:n.7062+9G>A | |
| XM_006724474.2:c.7200+9G>A | XP_006724537.1:n.7200+9G>A | |
| XM_006724475.2:c.7200+9G>A | XP_006724538.1:n.7200+9G>A | |
| XM_011545467.1:c.7077+9G>A | XP_011543769.1:n.7077+9G>A | |
| XM_011545468.1:c.7200+9G>A | XP_011543770.1:n.7200+9G>A | |
| XM_006724469.3:c.7176+9G>A | XP_006724532.1:n.7176+9G>A | |
| XM_006724470.3:c.7200+9G>A | XP_006724533.1:n.7200+9G>A | |
| XM_006724474.3:c.7200+9G>A | XP_006724537.1:n.7200+9G>A | |
| XM_011545468.2:c.7200+9G>A | XP_011543770.1:n.7200+9G>A | |
| XM_017029328.1:c.7200+9G>A | XP_016884817.1:n.7200+9G>A | |
| XM_017029331.1:c.1374+9G>A | XP_016884820.1:n.1374+9G>A | |
| NM_000109.4:c.7176+9G>A | NP_000100.3:n.7176+9G>A | |
| NM_004006.3:c.7200+9G>A MANE Select | NP_003997.2:n.7200+9G>A | |
| NM_004011.4:c.3177+9G>A | NP_004002.3:n.3177+9G>A | |
| NM_004012.4:c.3168+9G>A | NP_004003.2:n.3168+9G>A | |
| NM_004021.3:c.-181+9G>A | NP_004012.2:n.-181+9G>A | |
| NM_004023.3:c.-181+9G>A | NP_004014.2:n.-181+9G>A | |
| NM_004013.3:c.-181+9G>A | NP_004004.2:n.-181+9G>A | |
| NM_004020.4:c.-181+9G>A | NP_004011.3:n.-181+9G>A | |
| NM_004022.3:c.-181+9G>A | NP_004013.2:n.-181+9G>A |