Linked Data
dbSNP Id:
rs762143783
ExAC:
9:4117734 A / G
gnomAD v2:
9-4117734-A-G
gnomAD v3:
9-4117734-A-G
gnomAD v4:
9-4117734-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.4117734A>G , CM000671.2:g.4117734A>G | GRCh38 |
| NC_000009.11:g.4117734A>G , CM000671.1:g.4117734A>G | GRCh37 |
| NC_000009.10:g.4107734A>G | NCBI36 |
| NG_011782.1:g.187302T>C | |
| NG_011782.2:g.187302T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000491889.6:c.*1073+34T>C | ENSP00000419914.1:n.*1073+34T>C | |
| ENST00000645252.2:n.152+33206T>C | ||
| ENST00000682749.1:c.1245+34T>C | ENSP00000507306.1:n.1245+34T>C | |
| ENST00000682846.1:c.131+8000T>C | ENSP00000507527.1:n.131+8000T>C | |
| ENST00000381971.8:c.1710+34T>C MANE Select | ENSP00000371398.3:n.1710+34T>C | |
| ENST00000645252.1:n.152+33206T>C | ||
| ENST00000324333.14:c.1245+34T>C | ENSP00000325494.10:n.1245+34T>C | |
| ENST00000381971.7:c.1710+34T>C | ENSP00000371398.3:n.1710+34T>C | |
| ENST00000467497.6:n.250+34T>C | ||
| NM_001042413.1:c.1710+34T>C | NP_001035878.1:n.1710+34T>C | |
| NM_152629.3:c.1245+34T>C | NP_689842.3:n.1245+34T>C | |
| XM_005251386.3:c.1245+34T>C | XP_005251443.1:n.1245+34T>C | |
| XM_005251387.3:c.1044+34T>C | XP_005251444.1:n.1044+34T>C | |
| XM_005251388.3:c.1044+34T>C | XP_005251445.1:n.1044+34T>C | |
| XM_005251389.3:c.1710+34T>C | XP_005251446.1:n.1710+34T>C | |
| XM_006716731.2:c.1710+34T>C | XP_006716794.1:n.1710+34T>C | |
| XM_011517763.1:c.1710+34T>C | XP_011516065.1:n.1710+34T>C | |
| XM_011517764.1:c.1710+34T>C | XP_011516066.1:n.1710+34T>C | |
| XM_011517765.1:c.1710+34T>C | XP_011516067.1:n.1710+34T>C | |
| XM_011517766.1:c.1245+34T>C | XP_011516068.1:n.1245+34T>C | |
| XM_011517767.1:c.1044+34T>C | XP_011516069.1:n.1044+34T>C | |
| XM_011517768.1:c.1710+34T>C | XP_011516070.1:n.1710+34T>C | |
| XM_011517769.1:c.1710+34T>C | XP_011516071.1:n.1710+34T>C | |
| XR_929206.1:n.2476+34T>C | ||
| XM_005251386.4:c.1245+34T>C | XP_005251443.1:n.1245+34T>C | |
| XM_005251387.4:c.1044+34T>C | XP_005251444.1:n.1044+34T>C | |
| XM_005251388.4:c.1044+34T>C | XP_005251445.1:n.1044+34T>C | |
| XM_005251389.5:c.1710+34T>C | XP_005251446.1:n.1710+34T>C | |
| XM_006716731.3:c.1710+34T>C | XP_006716794.1:n.1710+34T>C | |
| XM_011517763.2:c.1710+34T>C | XP_011516065.1:n.1710+34T>C | |
| XM_011517764.2:c.1710+34T>C | XP_011516066.1:n.1710+34T>C | |
| XM_011517765.2:c.1710+34T>C | XP_011516067.1:n.1710+34T>C | |
| XM_011517766.2:c.1245+34T>C | XP_011516068.1:n.1245+34T>C | |
| XM_011517767.3:c.1044+34T>C | XP_011516069.1:n.1044+34T>C | |
| XM_011517769.2:c.1710+34T>C | XP_011516071.1:n.1710+34T>C | |
| XM_017014361.1:c.1245+34T>C | XP_016869850.1:n.1245+34T>C | |
| XR_929206.2:n.2472+34T>C | ||
| NM_001042413.2:c.1710+34T>C MANE Select | NP_001035878.1:n.1710+34T>C | |
| NM_152629.4:c.1245+34T>C | NP_689842.3:n.1245+34T>C |