Linked Data
dbSNP Id:
rs1125777
gnomAD v2:
1-61831890-C-T
gnomAD v3:
1-61366218-C-T
gnomAD v4:
1-61366218-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.61366218C>T , CM000663.2:g.61366218C>T | GRCh38 |
| NC_000001.10:g.61831890C>T , CM000663.1:g.61831890C>T | GRCh37 |
| NC_000001.9:g.61604478C>T | NCBI36 |
| NG_011787.1:g.293945C>T | |
| NG_011787.2:g.293945C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000482020.2:c.946+6944C>T | ENSP00000474806.2:n.946+6944C>T | |
| ENST00000699964.1:c.922+6944C>T | ENSP00000514720.1:n.922+6944C>T | |
| ENST00000699965.1:c.946+6944C>T | ENSP00000514721.1:n.946+6944C>T | |
| ENST00000699966.1:c.946+6944C>T | ENSP00000514722.1:n.946+6944C>T | |
| ENST00000699967.1:c.701-17019C>T | ENSP00000514723.1:n.701-17019C>T | |
| ENST00000699968.1:c.421+6944C>T | ENSP00000514724.1:n.421+6944C>T | |
| ENST00000699986.1:c.880+6944C>T | ENSP00000514739.1:n.880+6944C>T | |
| ENST00000699987.1:c.1069+6944C>T | ENSP00000514740.1:n.1069+6944C>T | |
| ENST00000699993.1:c.946+6944C>T | ENSP00000514743.1:n.946+6944C>T | |
| ENST00000403491.8:c.946+6944C>T MANE Select | ENSP00000384523.3:n.946+6944C>T | |
| ENST00000655770.1:c.178+6944C>T | ENSP00000499326.1:n.178+6944C>T | |
| ENST00000657234.1:c.178+6944C>T | ENSP00000499693.1:n.178+6944C>T | |
| ENST00000662015.1:c.*516+6944C>T | ENSP00000499312.1:n.*516+6944C>T | |
| ENST00000663597.1:c.178+6944C>T | ENSP00000499597.1:n.178+6944C>T | |
| ENST00000664149.1:c.946+6944C>T | ENSP00000499651.1:n.946+6944C>T | |
| ENST00000664495.1:c.*1038+6944C>T | ENSP00000499306.1:n.*1038+6944C>T | |
| ENST00000670151.1:c.947-6479C>T | ENSP00000499729.1:n.947-6479C>T | |
| ENST00000371184.6:c.560-17019C>T | ENSP00000360226.1:n.560-17019C>T | |
| ENST00000371185.6:c.880+6944C>T | ENSP00000360227.1:n.880+6944C>T | |
| ENST00000371187.7:c.946+6944C>T | ENSP00000360229.3:n.946+6944C>T | |
| ENST00000371189.8:c.1081+6944C>T | ENSP00000360231.3:n.1081+6944C>T | |
| ENST00000371191.5:c.1015+6944C>T | ENSP00000360233.1:n.1015+6944C>T | |
| ENST00000403491.7:c.946+6944C>T | ENSP00000384523.3:n.946+6944C>T | |
| ENST00000407417.7:c.922+6944C>T | ENSP00000384680.2:n.922+6944C>T | |
| ENST00000479364.1:n.536+6944C>T | ||
| ENST00000482020.1:c.246+6944C>T | ||
| ENST00000485903.6:c.946+6944C>T | ENSP00000419785.2:n.946+6944C>T | |
| NM_001134673.3:c.946+6944C>T | NP_001128145.1:n.946+6944C>T | |
| NM_001145511.1:c.922+6944C>T | NP_001138983.1:n.922+6944C>T | |
| NM_001145512.1:c.1081+6944C>T | NP_001138984.1:n.1081+6944C>T | |
| NM_005595.4:c.946+6944C>T | NP_005586.1:n.946+6944C>T | |
| XM_011541512.1:c.946+6944C>T | XP_011539814.1:n.946+6944C>T | |
| XM_011541513.1:c.946+6944C>T | XP_011539815.1:n.946+6944C>T | |
| XM_011541514.1:c.922+6944C>T | XP_011539816.1:n.922+6944C>T | |
| XM_011541515.1:c.946+6944C>T | XP_011539817.1:n.946+6944C>T | |
| XM_011541512.3:c.946+6944C>T | XP_011539814.1:n.946+6944C>T | |
| XM_011541514.3:c.922+6944C>T | XP_011539816.1:n.922+6944C>T | |
| XM_011541515.3:c.946+6944C>T | XP_011539817.1:n.946+6944C>T | |
| XM_017001362.2:c.922+6944C>T | XP_016856851.1:n.922+6944C>T | |
| XM_017001363.1:c.178+6944C>T | XP_016856852.1:n.178+6944C>T | |
| NM_001134673.4:c.946+6944C>T MANE Select | NP_001128145.1:n.946+6944C>T | |
| NM_001145511.2:c.922+6944C>T | NP_001138983.1:n.922+6944C>T | |
| NM_001145512.2:c.1081+6944C>T | NP_001138984.1:n.1081+6944C>T | |
| NM_005595.5:c.946+6944C>T | NP_005586.1:n.946+6944C>T |