Linked Data
ClinVar Variation Id:
408387
dbSNP Id:
rs767424884
ExAC:
5:131911512 T / G
gnomAD v2:
5-131911512-T-G
gnomAD v3:
5-132575820-T-G
gnomAD v4:
5-132575820-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132575820T>G , CM000667.2:g.132575820T>G | GRCh38 |
| NC_000005.9:g.131911512T>G , CM000667.1:g.131911512T>G | GRCh37 |
| NC_000005.8:g.131939411T>G | NCBI36 |
| NG_021151.1:g.23897T>G | |
| NG_021151.2:g.23844T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378823.8:c.257T>G MANE Select | ENSP00000368100.4:p.Phe86Cys | |
| ENST00000638452.2:c.-41T>G | ENSP00000492349.2:n.-41T>G | |
| ENST00000638504.1:n.334T>G | ||
| ENST00000638568.2:c.-41T>G | ENSP00000491158.2:n.-41T>G | |
| ENST00000639899.1:n.417T>G | ||
| ENST00000640655.2:c.-41T>G | ENSP00000491596.2:n.-41T>G | |
| ENST00000651160.1:c.257T>G | ENSP00000498829.1:p.Phe86Cys | |
| ENST00000651541.1:c.-41T>G | ENSP00000498795.1:n.-41T>G | |
| ENST00000651658.1:n.325T>G | ||
| ENST00000651723.1:c.*405T>G | ENSP00000498237.1:n.*405T>G | |
| ENST00000652016.1:c.257T>G | ENSP00000498267.1:p.Phe86Cys | |
| ENST00000652485.1:c.257T>G | ENSP00000498973.1:p.Phe86Cys | |
| ENST00000378823.7:c.257T>G | ENSP00000368100.4:p.Phe86Cys | |
| ENST00000416135.5:c.-41T>G | ENSP00000389515.1:n.-41T>G | |
| ENST00000423956.5:c.257T>G | ENSP00000390971.1:p.Phe86Cys | |
| ENST00000453394.5:c.257T>G | ENSP00000400049.1:p.Phe86Cys | |
| ENST00000533482.5:c.257T>G | ENSP00000431225.1:p.Phe86Cys | |
| NM_005732.3:c.257T>G | NP_005723.2:p.Phe86Cys | |
| NM_005732.4:c.257T>G MANE Select | NP_005723.2:p.Phe86Cys |