Linked Data
ClinVar Variation Id:
326069
dbSNP Id:
rs373530008
ExAC:
17:8133650 G / A
gnomAD v2:
17-8133650-G-A
gnomAD v3:
17-8230332-G-A
gnomAD v4:
17-8230332-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8230332G>A , CM000679.2:g.8230332G>A | GRCh38 |
| NC_000017.10:g.8133650G>A , CM000679.1:g.8133650G>A | GRCh37 |
| NC_000017.9:g.8074375G>A | NCBI36 |
| NG_032148.1:g.22764C>T | |
| NG_032148.2:g.22764C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580299.2:c.2895C>T | ENSP00000462607.2:p.Ala965= | |
| ENST00000581729.2:c.2895C>T | ENSP00000462720.2:p.Ala965= | |
| ENST00000581967.2:n.3347C>T | ||
| ENST00000583254.2:n.4568C>T | ||
| ENST00000699849.1:c.1998C>T | ENSP00000514647.1:p.Ala666= | |
| ENST00000699850.1:n.2158C>T | ||
| ENST00000699851.1:n.2917C>T | ||
| ENST00000699852.1:c.*1473C>T | ENSP00000514648.1:n.*1473C>T | |
| ENST00000699853.1:c.2895C>T | ENSP00000514649.1:p.Ala965= | |
| ENST00000699854.1:n.2688C>T | ||
| ENST00000699855.1:n.3347C>T | ||
| ENST00000699856.1:c.2895C>T | ENSP00000514650.1:p.Ala965= | |
| ENST00000699857.1:n.2805C>T | ||
| ENST00000699858.1:c.*1508C>T | ENSP00000514651.1:n.*1508C>T | |
| ENST00000699859.1:c.2766C>T | ENSP00000514652.1:p.Ala922= | |
| ENST00000699860.1:n.807C>T | ||
| ENST00000699861.1:n.2917C>T | ||
| ENST00000699862.1:n.3855C>T | ||
| ENST00000449476.7:c.2790C>T | ENSP00000396018.2:p.Ala930= | |
| ENST00000581671.2:n.2884C>T | ||
| ENST00000643543.1:c.*1602C>T | ENSP00000494323.1:n.*1602C>T | |
| ENST00000651323.1:c.2895C>T MANE Select | ENSP00000498499.1:p.Ala965= | |
| ENST00000315684.12:c.2895C>T | ENSP00000313759.8:p.Ala965= | |
| ENST00000449476.6:c.2790C>T | ENSP00000396018.2:p.Ala930= | |
| ENST00000578240.1:n.1123C>T | ||
| ENST00000578441.5:n.298C>T | ||
| ENST00000578537.1:c.597C>T | ||
| ENST00000580299.1:c.66C>T | ENSP00000462607.1:p.Ala22= | |
| ENST00000584439.1:n.508C>T | ||
| NM_025099.5:c.2895C>T | NP_079375.3:p.Ala965= | |
| NR_046431.1:n.2849C>T | ||
| XM_006721577.2:c.2766C>T | XP_006721640.1:p.Ala922= | |
| XM_006721578.2:c.2895C>T | XP_006721641.1:p.Ala965= | |
| XM_006721579.2:c.2895C>T | XP_006721642.1:p.Ala965= | |
| XM_011524010.1:c.2790C>T | XP_011522312.1:p.Ala930= | |
| XM_011524011.1:c.1998C>T | XP_011522313.1:p.Ala666= | |
| XR_429823.2:n.2938C>T | ||
| XR_429824.2:n.2938C>T | ||
| XR_429825.1:n.2744C>T | ||
| NM_025099.6:c.2895C>T MANE Select | NP_079375.3:p.Ala965= | |
| XM_006721577.3:c.2766C>T | XP_006721640.1:p.Ala922= | |
| XM_006721578.3:c.2895C>T | XP_006721641.1:p.Ala965= | |
| XM_011524010.2:c.2790C>T | XP_011522312.1:p.Ala930= | |
| XM_011524011.2:c.1998C>T | XP_011522313.1:p.Ala666= | |
| XR_001752639.1:n.2809C>T | ||
| XR_001752640.1:n.2938C>T | ||
| XR_001752641.1:n.2938C>T | ||
| XR_001752642.1:n.2744C>T | ||
| XR_001752643.1:n.3368C>T | ||
| XR_002958073.1:n.2744C>T | ||
| XR_429823.3:n.2938C>T | ||
| XR_429824.3:n.2938C>T | ||
| NR_046431.2:n.2810C>T |