Linked Data
ClinVar Variation Id:
542290
dbSNP Id:
rs764379949
ExAC:
22:31336810 G / A
gnomAD v2:
22-31336810-G-A
gnomAD v3:
22-30940823-G-A
gnomAD v4:
22-30940823-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.30940823G>A , CM000684.2:g.30940823G>A | GRCh38 |
| NC_000022.10:g.31336810G>A , CM000684.1:g.31336810G>A | GRCh37 |
| NC_000022.9:g.29666810G>A | NCBI36 |
| NG_046752.1:g.32675C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397641.8:c.839C>T MANE Select | ENSP00000380763.2:p.Thr280Met | |
| ENST00000675601.1:n.681C>T | ||
| ENST00000676215.1:n.15C>T | ||
| ENST00000215862.8:c.653C>T | ENSP00000215862.4:p.Thr218Met | |
| ENST00000397641.7:c.839C>T | ENSP00000380763.2:p.Thr280Met | |
| ENST00000469915.1:n.393C>T | ||
| NM_001303256.1:c.839C>T | NP_001290185.1:p.Thr280Met | |
| NM_001303257.1:c.839C>T | NP_001290186.1:p.Thr280Met | |
| NM_014941.2:c.653C>T | NP_055756.1:p.Thr218Met | |
| XM_011530003.1:c.863C>T | XP_011528305.1:p.Thr288Met | |
| XM_011530004.1:c.854C>T | XP_011528306.1:p.Thr285Met | |
| XM_011530005.1:c.863C>T | XP_011528307.1:p.Thr288Met | |
| XM_011530006.1:c.704C>T | XP_011528308.1:p.Thr235Met | |
| NM_001303256.2:c.839C>T | NP_001290185.1:p.Thr280Met | |
| NM_001303257.2:c.839C>T | NP_001290186.1:p.Thr280Met | |
| NM_014941.3:c.653C>T | NP_055756.1:p.Thr218Met | |
| XM_011530004.2:c.854C>T | XP_011528306.1:p.Thr285Met | |
| XM_017028667.2:c.854C>T | XP_016884156.1:p.Thr285Met | |
| NM_001303256.3:c.839C>T MANE Select | NP_001290185.1:p.Thr280Met |