Linked Data
ClinVar Variation Id:
224519
dbSNP Id:
rs869312756
gnomAD v4:
11-108307985-G-T
PubMed:
PMID:26845104
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108307985G>T , CM000673.2:g.108307985G>T | GRCh38 |
| NC_000011.9:g.108178712G>T , CM000673.1:g.108178712G>T | GRCh37 |
| NC_000011.8:g.107683922G>T | NCBI36 |
| NG_009830.1:g.90154G>T , LRG_135:g.90154G>T | |
| NG_054724.1:g.166848C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.5762+1G>T | ENSP00000388058.2:n.5762+1G>T | |
| ENST00000713593.1:c.*5233+1G>T | ENSP00000518889.1:n.*5233+1G>T | |
| ENST00000278616.9:c.5762+1G>T | ENSP00000278616.4:n.5762+1G>T | |
| ENST00000525056.2:n.181+1G>T | ||
| ENST00000682286.1:n.519+1G>T | ||
| ENST00000682302.1:n.180+1G>T | ||
| ENST00000683174.1:n.7246+1G>T | ||
| ENST00000683524.1:n.986+1G>T | ||
| ENST00000684152.1:n.1476+1G>T | ||
| ENST00000527805.6:c.*826+1G>T | ENSP00000435747.2:n.*826+1G>T | |
| ENST00000675595.1:c.*826+1G>T | ENSP00000502563.1:n.*826+1G>T | |
| ENST00000675843.1:c.5762+1G>T MANE Select | ENSP00000501606.1:n.5762+1G>T | |
| ENST00000278616.8:c.5762+1G>T | ENSP00000278616.4:n.5762+1G>T | |
| ENST00000452508.6:c.5762+1G>T | ENSP00000388058.2:n.5762+1G>T | |
| ENST00000524792.5:n.1977+1G>T | ||
| ENST00000529588.5:c.187-2175G>T | ||
| ENST00000533690.5:n.1166+1G>T | ||
| NM_000051.3:c.5762+1G>T , LRG_135t1:c.5762+1G>T | NP_000042.3:n.5762+1G>T | |
| XM_005271561.3:c.5762+1G>T | XP_005271618.2:n.5762+1G>T | |
| XM_005271562.3:c.5762+1G>T | XP_005271619.2:n.5762+1G>T | |
| XM_006718843.2:c.5762+1G>T | XP_006718906.1:n.5762+1G>T | |
| XM_006718845.1:c.1718+1G>T | XP_006718908.1:n.1718+1G>T | |
| XM_011542840.1:c.5762+1G>T | XP_011541142.1:n.5762+1G>T | |
| XM_011542841.1:c.5762+1G>T | XP_011541143.1:n.5762+1G>T | |
| XM_011542842.1:c.5597+1G>T | XP_011541144.1:n.5597+1G>T | |
| XM_011542843.1:c.5762+1G>T | XP_011541145.1:n.5762+1G>T | |
| XM_011542844.1:c.4718+1G>T | XP_011541146.1:n.4718+1G>T | |
| XM_011542845.1:c.4454+1G>T | XP_011541147.1:n.4454+1G>T | |
| XM_011542847.1:c.833+1G>T | XP_011541149.1:n.833+1G>T | |
| NM_001351834.1:c.5762+1G>T | NP_001338763.1:n.5762+1G>T | |
| XM_005271562.5:c.5762+1G>T | XP_005271619.2:n.5762+1G>T | |
| XM_006718843.4:c.5762+1G>T | XP_006718906.1:n.5762+1G>T | |
| XM_006718845.2:c.1718+1G>T | XP_006718908.1:n.1718+1G>T | |
| XM_011542840.3:c.5762+1G>T | XP_011541142.1:n.5762+1G>T | |
| XM_011542842.3:c.5597+1G>T | XP_011541144.1:n.5597+1G>T | |
| XM_011542843.2:c.5762+1G>T | XP_011541145.1:n.5762+1G>T | |
| XM_011542844.3:c.4718+1G>T | XP_011541146.1:n.4718+1G>T | |
| XM_011542845.2:c.4454+1G>T | XP_011541147.1:n.4454+1G>T | |
| XM_017017789.2:c.5762+1G>T | XP_016873278.1:n.5762+1G>T | |
| XM_017017790.2:c.5762+1G>T | XP_016873279.1:n.5762+1G>T | |
| XM_017017791.1:c.5762+1G>T | XP_016873280.1:n.5762+1G>T | |
| XR_002957150.1:n.6362+1G>T | ||
| NM_001351834.2:c.5762+1G>T | NP_001338763.1:n.5762+1G>T | |
| NM_000051.4:c.5762+1G>T MANE Select | NP_000042.3:n.5762+1G>T |