Linked Data
ClinVar Variation Id:
224118
dbSNP Id:
rs369160589
ExAC:
16:5132677 A / G
gnomAD v2:
16-5132677-A-G
gnomAD v3:
16-5082676-A-G
gnomAD v4:
16-5082676-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.5082676A>G , CM000678.2:g.5082676A>G | GRCh38 |
| NC_000016.9:g.5132677A>G , CM000678.1:g.5132677A>G | GRCh37 |
| NC_000016.8:g.5072678A>G | NCBI36 |
| NG_009202.1:g.15868A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592793.6:n.3323+3A>G | ||
| ENST00000682020.1:c.593+3A>G | ENSP00000508075.1:n.593+3A>G | |
| ENST00000682206.1:c.*282+3A>G | ENSP00000508285.1:n.*282+3A>G | |
| ENST00000682314.1:n.1238A>G | ||
| ENST00000682327.1:c.659+3A>G | ENSP00000507058.1:n.659+3A>G | |
| ENST00000682349.1:n.3329+3A>G | ||
| ENST00000682703.1:n.4158A>G | ||
| ENST00000682797.1:c.*279+3A>G | ENSP00000507582.1:n.*279+3A>G | |
| ENST00000682985.1:c.698+3A>G | ENSP00000507598.1:n.698+3A>G | |
| ENST00000683433.1:c.446+3A>G | ENSP00000507463.1:n.446+3A>G | |
| ENST00000683685.1:n.2064A>G | ||
| ENST00000683710.1:c.*1154+3A>G | ENSP00000506785.1:n.*1154+3A>G | |
| ENST00000683739.1:c.854+3A>G | ENSP00000507002.1:n.854+3A>G | |
| ENST00000683772.1:n.1234A>G | ||
| ENST00000684008.1:c.1125+3A>G | ENSP00000507962.1:n.1125+3A>G | |
| ENST00000684190.1:c.1148+3A>G | ENSP00000507554.1:n.1148+3A>G | |
| ENST00000684335.1:c.1076+3A>G | ENSP00000508112.1:n.1076+3A>G | |
| ENST00000262374.10:c.1187+3A>G MANE Select | ENSP00000262374.5:n.1187+3A>G | |
| ENST00000650085.1:n.2011+3A>G | ||
| ENST00000262374.9:c.1187+3A>G | ENSP00000262374.4:n.1187+3A>G | |
| ENST00000544428.1:c.854+3A>G | ENSP00000440019.1:n.854+3A>G | |
| ENST00000588623.5:c.854+3A>G | ENSP00000468118.1:n.854+3A>G | |
| ENST00000591822.5:c.*1088+3A>G | ENSP00000467865.1:n.*1088+3A>G | |
| NM_019109.4:c.1187+3A>G | NP_061982.3:n.1187+3A>G | |
| XM_011522565.1:c.854+3A>G | XP_011520867.1:n.854+3A>G | |
| NM_001330504.1:c.854+3A>G | NP_001317433.1:n.854+3A>G | |
| XM_017023457.2:c.1148+3A>G | XP_016878946.1:n.1148+3A>G | |
| XM_017023458.1:c.854+3A>G | XP_016878947.1:n.854+3A>G | |
| XR_932882.3:n.1216+3A>G | ||
| NM_019109.5:c.1187+3A>G MANE Select | NP_061982.3:n.1187+3A>G | |
| NM_001330504.2:c.854+3A>G | NP_001317433.1:n.854+3A>G |