Linked Data
ClinVar Variation Id:
2040098
ClinVar RCV Id:
RCV002886253
dbSNP Id:
rs121908140
gnomAD v2:
3-150645894-A-T
gnomAD v4:
3-150928107-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150928107A>T , CM000665.2:g.150928107A>T | GRCh38 |
| NC_000003.11:g.150645894A>T , CM000665.1:g.150645894A>T | GRCh37 |
| NC_000003.10:g.152128584A>T | NCBI36 |
| NG_009168.1:g.49893T>A , LRG_700:g.49893T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327047.6:c.528T>A MANE Select | ENSP00000322280.1:p.Tyr176Ter | |
| ENST00000468836.2:c.676T>A | ENSP00000419892.2:n.676T>A | |
| ENST00000295911.6:c.300T>A | ENSP00000295911.2:p.Tyr100Ter | |
| ENST00000327047.5:c.528T>A | ENSP00000322280.1:p.Tyr176Ter | |
| ENST00000328863.8:c.567T>A | ENSP00000329158.4:p.Tyr189Ter | |
| ENST00000468836.1:c.300T>A | ENSP00000419892.1:p.Tyr100Ter | |
| ENST00000562308.5:c.104+13475T>A | ||
| ENST00000565169.1:c.162+13475T>A | ||
| ENST00000569170.5:c.162+13475T>A | ||
| NM_001195794.1:c.567T>A , LRG_700t1:c.567T>A | NP_001182723.1:p.Tyr189Ter | |
| NM_001256819.1:c.*142T>A | NP_001243748.1:n.*142T>A | |
| NM_052995.2:c.300T>A , LRG_700t2:c.300T>A | NP_443721.1:p.Tyr100Ter | |
| NM_174878.2:c.528T>A | NP_777367.1:p.Tyr176Ter | |
| NR_046380.2:n.1009T>A | ||
| XR_924167.1:n.840T>A | ||
| NM_001256819.2:c.*142T>A | NP_001243748.1:n.*142T>A | |
| NM_174878.3:c.528T>A MANE Select | NP_777367.1:p.Tyr176Ter | |
| NR_046380.3:n.737T>A |