Linked Data
ClinVar Variation Id:
205183
dbSNP Id:
rs150001589
ExAC:
15:68506647 G / A
gnomAD v2:
15-68506647-G-A
gnomAD v3:
15-68214309-G-A
gnomAD v4:
15-68214309-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68214309G>A , CM000677.2:g.68214309G>A | GRCh38 |
| NC_000015.9:g.68506647G>A , CM000677.1:g.68506647G>A | GRCh37 |
| NC_000015.8:g.66293701G>A | NCBI36 |
| NG_008764.2:g.47903C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.278C>T MANE Select | ENSP00000249806.5:p.Thr93Met | |
| ENST00000562767.2:c.83+15193C>T | ENSP00000456336.1:n.83+15193C>T | |
| ENST00000563917.2:n.120C>T | ||
| ENST00000565471.6:c.84-4550C>T | ENSP00000457384.1:n.84-4550C>T | |
| ENST00000635747.1:c.*181C>T | ENSP00000490627.1:n.*181C>T | |
| ENST00000635754.1:n.1300C>T | ||
| ENST00000636020.1:n.410C>T | ||
| ENST00000636212.1:c.278C>T | ENSP00000489851.1:p.Thr93Met | |
| ENST00000636314.1:c.163C>T | ENSP00000490295.1:p.Arg55Cys | |
| ENST00000637054.1:c.198+4227C>T | ENSP00000490807.1:n.198+4227C>T | |
| ENST00000637223.1:c.*181C>T | ENSP00000490010.1:n.*181C>T | |
| ENST00000637329.1:c.189C>T | ||
| ENST00000637450.1:c.163C>T | ENSP00000490204.1:p.Arg55Cys | |
| ENST00000637494.1:c.199-2991C>T | ENSP00000490057.1:n.199-2991C>T | |
| ENST00000637667.1:c.199-2446C>T | ENSP00000489843.1:n.199-2446C>T | |
| ENST00000637823.1:c.204C>T | ||
| ENST00000637888.1:c.198+4227C>T | ENSP00000490546.1:n.198+4227C>T | |
| ENST00000638076.1:c.278C>T | ENSP00000490373.1:p.Thr93Met | |
| ENST00000638144.1:n.110C>T | ||
| ENST00000646164.1:c.38+4227C>T | ||
| ENST00000249806.9:c.278C>T | ENSP00000249806.5:p.Thr93Met | |
| ENST00000538696.5:c.374C>T | ENSP00000445770.1:p.Thr125Met | |
| ENST00000562767.1:c.83+15193C>T | ENSP00000456336.1:n.83+15193C>T | |
| ENST00000563917.1:n.59C>T | ||
| ENST00000564752.1:c.278C>T | ENSP00000457822.1:p.Thr93Met | |
| ENST00000564846.1:n.710C>T | ||
| ENST00000565471.5:c.84-4550C>T | ENSP00000457384.1:n.84-4550C>T | |
| ENST00000566347.5:c.278C>T | ENSP00000457783.1:p.Thr93Met | |
| ENST00000567060.5:c.278C>T | ENSP00000454818.1:p.Thr93Met | |
| NM_017882.2:c.278C>T | NP_060352.1:p.Thr93Met | |
| XR_931861.1:n.381C>T | ||
| NM_017882.3:c.278C>T MANE Select | NP_060352.1:p.Thr93Met |