Linked Data
ClinVar Variation Id:
290671
dbSNP Id:
rs150378645
ExAC:
21:47423697 G / A
gnomAD v2:
21-47423697-G-A
gnomAD v3:
21-46003783-G-A
gnomAD v4:
21-46003783-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.46003783G>A , CM000683.2:g.46003783G>A | GRCh38 |
| NC_000021.8:g.47423697G>A , CM000683.1:g.47423697G>A | GRCh37 |
| NC_000021.7:g.46248125G>A | NCBI36 |
| NG_008674.1:g.27035G>A , LRG_475:g.27035G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463060.6:n.1256G>A | ||
| ENST00000612273.2:c.983G>A | ||
| ENST00000682634.1:c.983G>A | ||
| ENST00000361866.8:c.2857G>A MANE Select | ENSP00000355180.3:p.Ala953Thr | |
| ENST00000361866.7:c.2857G>A | ENSP00000355180.3:p.Ala953Thr | |
| ENST00000486023.1:n.645G>A | ||
| ENST00000498614.5:n.1091G>A | ||
| ENST00000612273.1:c.2851G>A | ENSP00000483630.1:p.Ala951Thr | |
| NM_001848.2:c.2857G>A , LRG_475t1:c.2857G>A | NP_001839.2:p.Ala953Thr | |
| NM_001848.3:c.2857G>A MANE Select | NP_001839.2:p.Ala953Thr |