Linked Data
ClinVar Variation Id:
568339
ClinVar RCV Id:
RCV000688665
dbSNP Id:
rs1565486050
gnomAD v4:
11-108307926-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108307926G>T , CM000673.2:g.108307926G>T | GRCh38 |
| NC_000011.9:g.108178653G>T , CM000673.1:g.108178653G>T | GRCh37 |
| NC_000011.8:g.107683863G>T | NCBI36 |
| NG_009830.1:g.90095G>T , LRG_135:g.90095G>T | |
| NG_054724.1:g.166907C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.5704G>T | ENSP00000388058.2:p.Asp1902Tyr | |
| ENST00000713593.1:c.*5175G>T | ENSP00000518889.1:n.*5175G>T | |
| ENST00000278616.9:c.5704G>T | ENSP00000278616.4:p.Asp1902Tyr | |
| ENST00000525056.2:n.123G>T | ||
| ENST00000682286.1:n.461G>T | ||
| ENST00000682302.1:n.122G>T | ||
| ENST00000683174.1:n.7188G>T | ||
| ENST00000683524.1:n.928G>T | ||
| ENST00000684152.1:n.1418G>T | ||
| ENST00000527805.6:c.*768G>T | ENSP00000435747.2:n.*768G>T | |
| ENST00000675595.1:c.*768G>T | ENSP00000502563.1:n.*768G>T | |
| ENST00000675843.1:c.5704G>T MANE Select | ENSP00000501606.1:p.Asp1902Tyr | |
| ENST00000278616.8:c.5704G>T | ENSP00000278616.4:p.Asp1902Tyr | |
| ENST00000452508.6:c.5704G>T | ENSP00000388058.2:p.Asp1902Tyr | |
| ENST00000524792.5:n.1919G>T | ||
| ENST00000529588.5:c.187-2234G>T | ||
| ENST00000533690.5:n.1108G>T | ||
| NM_000051.3:c.5704G>T , LRG_135t1:c.5704G>T | NP_000042.3:p.Asp1902Tyr | |
| XM_005271561.3:c.5704G>T | XP_005271618.2:p.Asp1902Tyr | |
| XM_005271562.3:c.5704G>T | XP_005271619.2:p.Asp1902Tyr | |
| XM_006718843.2:c.5704G>T | XP_006718906.1:p.Asp1902Tyr | |
| XM_006718845.1:c.1660G>T | XP_006718908.1:p.Asp554Tyr | |
| XM_011542840.1:c.5704G>T | XP_011541142.1:p.Asp1902Tyr | |
| XM_011542841.1:c.5704G>T | XP_011541143.1:p.Asp1902Tyr | |
| XM_011542842.1:c.5539G>T | XP_011541144.1:p.Asp1847Tyr | |
| XM_011542843.1:c.5704G>T | XP_011541145.1:p.Asp1902Tyr | |
| XM_011542844.1:c.4660G>T | XP_011541146.1:p.Asp1554Tyr | |
| XM_011542845.1:c.4396G>T | XP_011541147.1:p.Asp1466Tyr | |
| XM_011542847.1:c.775G>T | XP_011541149.1:p.Asp259Tyr | |
| NM_001351834.1:c.5704G>T | NP_001338763.1:p.Asp1902Tyr | |
| XM_005271562.5:c.5704G>T | XP_005271619.2:p.Asp1902Tyr | |
| XM_006718843.4:c.5704G>T | XP_006718906.1:p.Asp1902Tyr | |
| XM_006718845.2:c.1660G>T | XP_006718908.1:p.Asp554Tyr | |
| XM_011542840.3:c.5704G>T | XP_011541142.1:p.Asp1902Tyr | |
| XM_011542842.3:c.5539G>T | XP_011541144.1:p.Asp1847Tyr | |
| XM_011542843.2:c.5704G>T | XP_011541145.1:p.Asp1902Tyr | |
| XM_011542844.3:c.4660G>T | XP_011541146.1:p.Asp1554Tyr | |
| XM_011542845.2:c.4396G>T | XP_011541147.1:p.Asp1466Tyr | |
| XM_017017789.2:c.5704G>T | XP_016873278.1:p.Asp1902Tyr | |
| XM_017017790.2:c.5704G>T | XP_016873279.1:p.Asp1902Tyr | |
| XM_017017791.1:c.5704G>T | XP_016873280.1:p.Asp1902Tyr | |
| XR_002957150.1:n.6304G>T | ||
| NM_001351834.2:c.5704G>T | NP_001338763.1:p.Asp1902Tyr | |
| NM_000051.4:c.5704G>T MANE Select | NP_000042.3:p.Asp1902Tyr |