Linked Data
ClinVar Variation Id:
382580
dbSNP Id:
rs144029725
ExAC:
16:5129069 C / T
gnomAD v2:
16-5129069-C-T
gnomAD v3:
16-5079068-C-T
gnomAD v4:
16-5079068-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.5079068C>T , CM000678.2:g.5079068C>T | GRCh38 |
| NC_000016.9:g.5129069C>T , CM000678.1:g.5129069C>T | GRCh37 |
| NC_000016.8:g.5069070C>T | NCBI36 |
| NG_009202.1:g.12260C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000592793.6:n.3003C>T | ||
| ENST00000682020.1:c.273C>T | ENSP00000508075.1:p.Asp91= | |
| ENST00000682206.1:c.867C>T | ENSP00000508285.1:p.Asp289= | |
| ENST00000682314.1:n.911C>T | ||
| ENST00000682327.1:c.373+190C>T | ENSP00000507058.1:n.373+190C>T | |
| ENST00000682349.1:n.3005C>T | ||
| ENST00000682703.1:n.3190C>T | ||
| ENST00000682797.1:c.867C>T | ENSP00000507582.1:p.Asp289= | |
| ENST00000682985.1:c.378C>T | ENSP00000507598.1:p.Asp126= | |
| ENST00000683433.1:c.157+190C>T | ENSP00000507463.1:n.157+190C>T | |
| ENST00000683685.1:n.1096C>T | ||
| ENST00000683710.1:c.*830C>T | ENSP00000506785.1:n.*830C>T | |
| ENST00000683739.1:c.534C>T | ENSP00000507002.1:p.Asp178= | |
| ENST00000683772.1:n.911C>T | ||
| ENST00000684008.1:c.801C>T | ENSP00000507962.1:p.Asp267= | |
| ENST00000684190.1:c.862+190C>T | ENSP00000507554.1:n.862+190C>T | |
| ENST00000684335.1:c.867C>T | ENSP00000508112.1:p.Asp289= | |
| ENST00000262374.10:c.867C>T MANE Select | ENSP00000262374.5:p.Asp289= | |
| ENST00000650085.1:n.1687C>T | ||
| ENST00000262374.9:c.867C>T | ENSP00000262374.4:p.Asp289= | |
| ENST00000544428.1:c.534C>T | ENSP00000440019.1:p.Asp178= | |
| ENST00000588623.5:c.534C>T | ENSP00000468118.1:p.Asp178= | |
| ENST00000591822.5:c.*768C>T | ENSP00000467865.1:n.*768C>T | |
| NM_019109.4:c.867C>T | NP_061982.3:p.Asp289= | |
| XM_011522565.1:c.534C>T | XP_011520867.1:p.Asp178= | |
| XR_932882.1:n.908C>T | ||
| NM_001330504.1:c.534C>T | NP_001317433.1:p.Asp178= | |
| XM_017023457.2:c.862+190C>T | XP_016878946.1:n.862+190C>T | |
| XM_017023458.1:c.534C>T | XP_016878947.1:p.Asp178= | |
| XR_932882.3:n.892C>T | ||
| NM_019109.5:c.867C>T MANE Select | NP_061982.3:p.Asp289= | |
| NM_001330504.2:c.534C>T | NP_001317433.1:p.Asp178= |