Linked Data
ClinVar Variation Id:
326071
dbSNP Id:
rs200759730
ExAC:
17:8135080 C / T
gnomAD v2:
17-8135080-C-T
gnomAD v3:
17-8231762-C-T
gnomAD v4:
17-8231762-C-T
COSMIC:
COSM2882165
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8231762C>T , CM000679.2:g.8231762C>T | GRCh38 |
| NC_000017.10:g.8135080C>T , CM000679.1:g.8135080C>T | GRCh37 |
| NC_000017.9:g.8075805C>T | NCBI36 |
| NG_032148.1:g.21334G>A | |
| NG_032148.2:g.21334G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580299.2:c.2439G>A | ENSP00000462607.2:p.Pro813= | |
| ENST00000581729.2:c.2439G>A | ENSP00000462720.2:p.Pro813= | |
| ENST00000581967.2:n.2891G>A | ||
| ENST00000583254.2:n.3232G>A | ||
| ENST00000699849.1:c.1542G>A | ENSP00000514647.1:p.Pro514= | |
| ENST00000699850.1:n.1702G>A | ||
| ENST00000699851.1:n.2461G>A | ||
| ENST00000699852.1:c.*1115G>A | ENSP00000514648.1:n.*1115G>A | |
| ENST00000699853.1:c.2439G>A | ENSP00000514649.1:p.Pro813= | |
| ENST00000699854.1:n.2232G>A | ||
| ENST00000699855.1:n.2891G>A | ||
| ENST00000699856.1:c.2439G>A | ENSP00000514650.1:p.Pro813= | |
| ENST00000699857.1:n.2447G>A | ||
| ENST00000699858.1:c.*1052G>A | ENSP00000514651.1:n.*1052G>A | |
| ENST00000699859.1:c.2310G>A | ENSP00000514652.1:p.Pro770= | |
| ENST00000699860.1:n.545G>A | ||
| ENST00000699861.1:n.2461G>A | ||
| ENST00000699862.1:n.3399G>A | ||
| ENST00000449476.7:c.2334G>A | ENSP00000396018.2:p.Pro778= | |
| ENST00000581671.2:n.2428G>A | ||
| ENST00000643543.1:c.*1146G>A | ENSP00000494323.1:n.*1146G>A | |
| ENST00000651323.1:c.2439G>A MANE Select | ENSP00000498499.1:p.Pro813= | |
| ENST00000315684.12:c.2439G>A | ENSP00000313759.8:p.Pro813= | |
| ENST00000449476.6:c.2334G>A | ENSP00000396018.2:p.Pro778= | |
| ENST00000578240.1:n.667G>A | ||
| ENST00000578537.1:c.335G>A | ||
| NM_025099.5:c.2439G>A | NP_079375.3:p.Pro813= | |
| NR_046431.1:n.2393G>A | ||
| XM_006721577.2:c.2310G>A | XP_006721640.1:p.Pro770= | |
| XM_006721578.2:c.2439G>A | XP_006721641.1:p.Pro813= | |
| XM_006721579.2:c.2439G>A | XP_006721642.1:p.Pro813= | |
| XM_011524010.1:c.2334G>A | XP_011522312.1:p.Pro778= | |
| XM_011524011.1:c.1542G>A | XP_011522313.1:p.Pro514= | |
| XR_429823.2:n.2482G>A | ||
| XR_429824.2:n.2482G>A | ||
| XR_429825.1:n.2482G>A | ||
| NM_025099.6:c.2439G>A MANE Select | NP_079375.3:p.Pro813= | |
| XM_006721577.3:c.2310G>A | XP_006721640.1:p.Pro770= | |
| XM_006721578.3:c.2439G>A | XP_006721641.1:p.Pro813= | |
| XM_011524010.2:c.2334G>A | XP_011522312.1:p.Pro778= | |
| XM_011524011.2:c.1542G>A | XP_011522313.1:p.Pro514= | |
| XR_001752639.1:n.2353G>A | ||
| XR_001752640.1:n.2482G>A | ||
| XR_001752641.1:n.2482G>A | ||
| XR_001752642.1:n.2482G>A | ||
| XR_001752643.1:n.2912G>A | ||
| XR_002958073.1:n.2482G>A | ||
| XR_429823.3:n.2482G>A | ||
| XR_429824.3:n.2482G>A | ||
| NR_046431.2:n.2354G>A |