Linked Data
ClinVar Variation Id:
1497022
ClinVar RCV Id:
RCV002019724
dbSNP Id:
rs752902567
ExAC:
20:17474774 G / A
gnomAD v2:
20-17474774-G-A
gnomAD v4:
20-17494129-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.17494129G>A , CM000682.2:g.17494129G>A | GRCh38 |
| NC_000020.10:g.17474774G>A , CM000682.1:g.17474774G>A | GRCh37 |
| NC_000020.9:g.17422774G>A | NCBI36 |
| NG_012423.2:g.80092C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377873.8:c.1943C>T MANE Select | ENSP00000367104.3:p.Thr648Ile | |
| ENST00000536626.7:c.1526C>T | ENSP00000442522.1:p.Thr509Ile | |
| ENST00000377868.6:c.1568C>T | ENSP00000367099.2:p.Thr523Ile | |
| ENST00000377873.7:c.1943C>T | ENSP00000367104.3:p.Thr648Ile | |
| ENST00000536626.5:c.1526C>T | ENSP00000442522.1:p.Thr509Ile | |
| NM_001161705.1:c.1568C>T | NP_001155177.1:p.Thr523Ile | |
| NM_001195.4:c.1943C>T | NP_001186.1:p.Thr648Ile | |
| NM_001278606.1:c.1526C>T | NP_001265535.1:p.Thr509Ile | |
| NM_001278607.1:c.1610C>T | NP_001265536.1:p.Thr537Ile | |
| NM_001278608.1:c.1526C>T | NP_001265537.1:p.Thr509Ile | |
| XM_011529312.1:c.1526C>T | XP_011527614.1:p.Thr509Ile | |
| XM_017028005.2:c.1835C>T | XP_016883494.1:p.Thr612Ile | |
| NM_001195.5:c.1943C>T MANE Select | NP_001186.1:p.Thr648Ile | |
| NM_001161705.2:c.1568C>T | NP_001155177.1:p.Thr523Ile | |
| NM_001278606.2:c.1526C>T | NP_001265535.1:p.Thr509Ile | |
| NM_001278607.2:c.1610C>T | NP_001265536.1:p.Thr537Ile | |
| NM_001278608.2:c.1526C>T | NP_001265537.1:p.Thr509Ile |