Linked Data
ClinVar Variation Id:
382590
dbSNP Id:
rs61736264
ExAC:
1:154960937 C / T
gnomAD v2:
1-154960937-C-T
gnomAD v3:
1-154988461-C-T
gnomAD v4:
1-154988461-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154988461C>T , CM000663.2:g.154988461C>T | GRCh38 |
| NC_000001.10:g.154960937C>T , CM000663.1:g.154960937C>T | GRCh37 |
| NC_000001.9:g.153227561C>T | NCBI36 |
| NG_042310.1:g.10168C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000292180.8:c.729C>T MANE Select | ENSP00000292180.3:p.Phe243= | |
| ENST00000292180.7:c.729C>T | ENSP00000292180.3:p.Phe243= | |
| ENST00000295530.6:c.-73C>T | ENSP00000295530.2:n.-73C>T | |
| ENST00000315144.14:c.438C>T | ENSP00000317296.10:p.Phe146= | |
| ENST00000368431.7:c.432C>T | ENSP00000357416.3:p.Phe144= | |
| ENST00000368432.5:c.438C>T | ENSP00000357417.1:p.Phe146= | |
| ENST00000368433.5:c.729C>T | ENSP00000357418.1:p.Phe243= | |
| NM_001184891.1:c.438C>T | NP_001171820.1:p.Phe146= | |
| NM_001184892.1:c.432C>T | NP_001171821.1:p.Phe144= | |
| NM_025207.4:c.729C>T | NP_079483.3:p.Phe243= | |
| NM_201398.2:c.438C>T | NP_958800.1:p.Phe146= | |
| XM_005245502.2:c.438C>T | XP_005245559.1:p.Phe146= | |
| XM_005245503.2:c.-73C>T | XP_005245560.1:n.-73C>T | |
| XM_006711559.2:c.438C>T | XP_006711622.1:p.Phe146= | |
| XR_241098.3:n.647C>T | ||
| NM_025207.5:c.729C>T MANE Select | NP_079483.3:p.Phe243= | |
| NM_001184891.2:c.438C>T | NP_001171820.1:p.Phe146= | |
| NM_001184892.2:c.432C>T | NP_001171821.1:p.Phe144= | |
| NM_201398.3:c.438C>T | NP_958800.1:p.Phe146= |