Linked Data
ClinVar Variation Id:
651993
dbSNP Id:
rs1387467529
gnomAD v2:
22-24176351-C-T
gnomAD v3:
22-23834164-C-T
gnomAD v4:
22-23834164-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23834164C>T , CM000684.2:g.23834164C>T | GRCh38 |
| NC_000022.10:g.24176351C>T , CM000684.1:g.24176351C>T | GRCh37 |
| NC_000022.9:g.22506351C>T | NCBI36 |
| NG_009303.1:g.52202C>T , LRG_520:g.52202C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263121.12:c.1004C>T | ENSP00000263121.8:p.Thr335Met | |
| ENST00000344921.11:c.1169C>T | ENSP00000340883.6:p.Thr390Met | |
| ENST00000407422.8:c.1115C>T | ENSP00000383984.3:p.Thr372Met | |
| ENST00000644036.2:c.1142C>T MANE Select | ENSP00000494049.2:p.Thr381Met | |
| ENST00000644462.1:c.1860C>T | ENSP00000494283.1:n.1860C>T | |
| ENST00000645799.1:n.2464C>T | ||
| ENST00000646723.1:n.3488C>T | ||
| ENST00000647057.1:c.*636C>T | ENSP00000494757.1:n.*636C>T | |
| ENST00000263121.11:c.1142C>T | ENSP00000263121.7:p.Thr381Met | |
| ENST00000344921.10:c.1169C>T | ENSP00000340883.6:p.Thr390Met | |
| ENST00000407082.3:c.1004C>T | ENSP00000385226.3:p.Thr335Met | |
| ENST00000407422.7:c.1115C>T | ENSP00000383984.3:p.Thr372Met | |
| NM_001007468.1:c.1115C>T | NP_001007469.1:p.Thr372Met | |
| NM_003073.3:c.1142C>T , LRG_520t1:c.1142C>T | NP_003064.2:p.Thr381Met | |
| XM_011530345.1:c.1196C>T | XP_011528647.1:p.Thr399Met | |
| XM_011530346.1:c.1169C>T | XP_011528648.1:p.Thr390Met | |
| NM_001007468.2:c.1115C>T | NP_001007469.1:p.Thr372Met | |
| NM_001317946.1:c.1169C>T | NP_001304875.1:p.Thr390Met | |
| NM_001362877.1:c.1196C>T | NP_001349806.1:p.Thr399Met | |
| NM_003073.4:c.1142C>T | NP_003064.2:p.Thr381Met | |
| NM_001007468.3:c.1115C>T | NP_001007469.1:p.Thr372Met | |
| NM_001317946.2:c.1169C>T | NP_001304875.1:p.Thr390Met | |
| NM_001362877.2:c.1196C>T | NP_001349806.1:p.Thr399Met | |
| NM_003073.5:c.1142C>T MANE Select | NP_003064.2:p.Thr381Met |