Linked Data
ClinVar Variation Id:
234172
dbSNP Id:
rs748840480
gnomAD v2:
11-108115754-G-T
gnomAD v3:
11-108245027-G-T
gnomAD v4:
11-108245027-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108245027G>T , CM000673.2:g.108245027G>T | GRCh38 |
| NC_000011.9:g.108115754G>T , CM000673.1:g.108115754G>T | GRCh37 |
| NC_000011.8:g.107620964G>T | NCBI36 |
| NG_009830.1:g.27196G>T , LRG_135:g.27196G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.901+1G>T | ENSP00000388058.2:n.901+1G>T | |
| ENST00000713593.1:c.*372+1G>T | ENSP00000518889.1:n.*372+1G>T | |
| ENST00000278616.9:c.901+1G>T | ENSP00000278616.4:n.901+1G>T | |
| ENST00000682516.1:n.1035+1G>T | ||
| ENST00000682956.1:n.1035+1G>T | ||
| ENST00000683100.1:n.3248+1G>T | ||
| ENST00000683174.1:n.1051+1G>T | ||
| ENST00000683605.1:n.396+1G>T | ||
| ENST00000684037.1:c.901+1G>T | ENSP00000508245.1:n.901+1G>T | |
| ENST00000684061.1:n.1035+1G>T | ||
| ENST00000684179.1:n.870+1G>T | ||
| ENST00000527805.6:c.901+1G>T | ENSP00000435747.2:n.901+1G>T | |
| ENST00000675595.1:c.736+1G>T | ENSP00000502563.1:n.736+1G>T | |
| ENST00000675843.1:c.901+1G>T MANE Select | ENSP00000501606.1:n.901+1G>T | |
| ENST00000278616.8:c.901+1G>T | ENSP00000278616.4:n.901+1G>T | |
| ENST00000452508.6:c.901+1G>T | ENSP00000388058.2:n.901+1G>T | |
| ENST00000527805.5:c.901+1G>T | ENSP00000435747.1:n.901+1G>T | |
| NM_000051.3:c.901+1G>T , LRG_135t1:c.901+1G>T | NP_000042.3:n.901+1G>T | |
| XM_005271561.3:c.901+1G>T | XP_005271618.2:n.901+1G>T | |
| XM_005271562.3:c.901+1G>T | XP_005271619.2:n.901+1G>T | |
| XM_006718843.2:c.901+1G>T | XP_006718906.1:n.901+1G>T | |
| XM_011542840.1:c.901+1G>T | XP_011541142.1:n.901+1G>T | |
| XM_011542841.1:c.901+1G>T | XP_011541143.1:n.901+1G>T | |
| XM_011542842.1:c.736+1G>T | XP_011541144.1:n.736+1G>T | |
| XM_011542843.1:c.901+1G>T | XP_011541145.1:n.901+1G>T | |
| XM_011542844.1:c.-144+1G>T | XP_011541146.1:n.-144+1G>T | |
| XM_011542846.1:c.901+1G>T | XP_011541148.1:n.901+1G>T | |
| NM_001351834.1:c.901+1G>T | NP_001338763.1:n.901+1G>T | |
| XM_005271562.5:c.901+1G>T | XP_005271619.2:n.901+1G>T | |
| XM_006718843.4:c.901+1G>T | XP_006718906.1:n.901+1G>T | |
| XM_011542840.3:c.901+1G>T | XP_011541142.1:n.901+1G>T | |
| XM_011542842.3:c.736+1G>T | XP_011541144.1:n.736+1G>T | |
| XM_011542843.2:c.901+1G>T | XP_011541145.1:n.901+1G>T | |
| XM_011542844.3:c.-144+1G>T | XP_011541146.1:n.-144+1G>T | |
| XM_017017789.2:c.901+1G>T | XP_016873278.1:n.901+1G>T | |
| XM_017017790.2:c.901+1G>T | XP_016873279.1:n.901+1G>T | |
| XM_017017791.1:c.901+1G>T | XP_016873280.1:n.901+1G>T | |
| XM_017017792.2:c.901+1G>T | XP_016873281.1:n.901+1G>T | |
| XR_002957150.1:n.1634+1G>T | ||
| NM_001351834.2:c.901+1G>T | NP_001338763.1:n.901+1G>T | |
| NM_000051.4:c.901+1G>T MANE Select | NP_000042.3:n.901+1G>T |