Linked Data
ClinVar Variation Id:
96141
dbSNP Id:
rs146125583
ExAC:
9:140648752 C / T
gnomAD v2:
9-140648752-C-T
gnomAD v3:
9-137754300-C-T
gnomAD v4:
9-137754300-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137754300C>T , CM000671.2:g.137754300C>T | GRCh38 |
| NC_000009.11:g.140648752C>T , CM000671.1:g.140648752C>T | GRCh37 |
| NC_000009.10:g.139768573C>T | NCBI36 |
| NG_011776.1:g.140309C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460843.6:c.1369+9C>T MANE Select | ENSP00000417980.1:n.1369+9C>T | |
| ENST00000629335.2:c.1369+9C>T | ENSP00000490056.1:n.1369+9C>T | |
| ENST00000636027.1:c.1255+9C>T | ENSP00000489961.1:n.1255+9C>T | |
| ENST00000637161.1:c.1276+9C>T | ENSP00000490328.1:n.1276+9C>T | |
| ENST00000637261.1:c.1409+9C>T | ENSP00000490815.1:n.1409+9C>T | |
| ENST00000637977.1:c.1314+9C>T | ||
| ENST00000638071.1:c.996+9C>T | ||
| ENST00000640639.1:c.538+9C>T | ENSP00000491823.1:n.538+9C>T | |
| ENST00000371394.6:c.*1104+9C>T | ENSP00000485945.1:n.*1104+9C>T | |
| ENST00000460843.5:c.1369+9C>T | ENSP00000417980.1:n.1369+9C>T | |
| ENST00000462484.5:c.1369+9C>T | ENSP00000417328.1:n.1369+9C>T | |
| ENST00000462942.3:c.226+9C>T | ENSP00000436107.1:n.226+9C>T | |
| ENST00000465566.2:c.61+9C>T | ENSP00000486261.1:n.61+9C>T | |
| ENST00000626066.2:c.1272+9C>T | ||
| ENST00000629808.2:c.462+9C>T | ||
| NM_001145527.1:c.1369+9C>T | NP_001138999.1:n.1369+9C>T | |
| NM_024757.4:c.1369+9C>T | NP_079033.4:n.1369+9C>T | |
| XM_005266105.3:c.1360+9C>T | XP_005266162.1:n.1360+9C>T | |
| XM_005266110.1:c.1276+9C>T | XP_005266167.1:n.1276+9C>T | |
| XM_006717288.2:c.1351+9C>T | XP_006717351.1:n.1351+9C>T | |
| XM_011519021.1:c.1378+9C>T | XP_011517323.1:n.1378+9C>T | |
| XM_011519022.1:c.1375+9C>T | XP_011517324.1:n.1375+9C>T | |
| XM_011519023.1:c.1357+9C>T | XP_011517325.1:n.1357+9C>T | |
| XM_011519024.1:c.1300+9C>T | XP_011517326.1:n.1300+9C>T | |
| XM_011519025.1:c.1276+9C>T | XP_011517327.1:n.1276+9C>T | |
| XM_011519026.1:c.1378+9C>T | XP_011517328.1:n.1378+9C>T | |
| XM_011519027.1:c.1378+9C>T | XP_011517329.1:n.1378+9C>T | |
| XM_011519028.1:c.1378+9C>T | XP_011517330.1:n.1378+9C>T | |
| XM_011519033.1:c.1357+9C>T | XP_011517335.1:n.1357+9C>T | |
| NM_001354259.1:c.1276+9C>T | NP_001341188.1:n.1276+9C>T | |
| NM_001354263.1:c.1348+9C>T | NP_001341192.1:n.1348+9C>T | |
| NM_001354611.1:c.1369+9C>T | NP_001341540.1:n.1369+9C>T | |
| NM_001354612.1:c.1276+9C>T | NP_001341541.1:n.1276+9C>T | |
| XM_005266105.5:c.1360+9C>T | XP_005266162.1:n.1360+9C>T | |
| XM_011519021.3:c.1378+9C>T | XP_011517323.1:n.1378+9C>T | |
| XM_011519022.3:c.1375+9C>T | XP_011517324.1:n.1375+9C>T | |
| XM_011519023.3:c.1357+9C>T | XP_011517325.1:n.1357+9C>T | |
| XM_017015134.1:c.1354+9C>T | XP_016870623.1:n.1354+9C>T | |
| XM_017015136.2:c.1270+9C>T | XP_016870625.1:n.1270+9C>T | |
| XM_017015137.1:c.1255+9C>T | XP_016870626.1:n.1255+9C>T | |
| XM_017015138.1:c.1255+9C>T | XP_016870627.1:n.1255+9C>T | |
| XM_024447674.1:c.1198+9C>T | XP_024303442.1:n.1198+9C>T | |
| XM_024447675.1:c.1276+9C>T | XP_024303443.1:n.1276+9C>T | |
| XM_024447676.1:c.493+9C>T | XP_024303444.1:n.493+9C>T | |
| XM_024447677.1:c.493+9C>T | XP_024303445.1:n.493+9C>T | |
| XM_024447678.1:c.1276+9C>T | XP_024303446.1:n.1276+9C>T | |
| XM_024447679.1:c.1276+9C>T | XP_024303447.1:n.1276+9C>T | |
| XM_024447680.1:c.1255+9C>T | XP_024303448.1:n.1255+9C>T | |
| NM_024757.5:c.1369+9C>T MANE Select | NP_079033.4:n.1369+9C>T | |
| NM_001145527.2:c.1369+9C>T | NP_001138999.1:n.1369+9C>T | |
| NM_001354259.2:c.1276+9C>T | NP_001341188.1:n.1276+9C>T | |
| NM_001354263.2:c.1348+9C>T | NP_001341192.1:n.1348+9C>T | |
| NM_001354611.2:c.1369+9C>T | NP_001341540.1:n.1369+9C>T | |
| NM_001354612.2:c.1276+9C>T | NP_001341541.1:n.1276+9C>T |