Linked Data
ClinVar Variation Id:
290280
dbSNP Id:
rs139701867
ExAC:
1:46662488 C / T
gnomAD v2:
1-46662488-C-T
gnomAD v3:
1-46196816-C-T
gnomAD v4:
1-46196816-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.46196816C>T , CM000663.2:g.46196816C>T | GRCh38 |
| NC_000001.10:g.46662488C>T , CM000663.1:g.46662488C>T | GRCh37 |
| NC_000001.9:g.46435075C>T | NCBI36 |
| NG_009205.2:g.28490G>A | |
| NG_009205.3:g.28490G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396420.8:c.269G>A | ENSP00000379698.4:p.Arg90His | |
| ENST00000477114.2:n.441G>A | ||
| ENST00000497439.6:n.441G>A | ||
| ENST00000684817.1:n.437G>A | ||
| ENST00000684898.1:n.441G>A | ||
| ENST00000685230.1:c.269G>A | ENSP00000510305.1:p.Arg90His | |
| ENST00000685275.1:n.426G>A | ||
| ENST00000685444.1:c.269G>A | ENSP00000510762.1:p.Arg90His | |
| ENST00000685704.1:n.441G>A | ||
| ENST00000685775.1:n.561G>A | ||
| ENST00000685833.1:n.414G>A | ||
| ENST00000686252.1:n.690G>A | ||
| ENST00000686379.1:c.269G>A | ENSP00000508913.1:p.Arg90His | |
| ENST00000686724.1:n.441G>A | ||
| ENST00000686737.1:c.269G>A | ENSP00000508736.1:p.Arg90His | |
| ENST00000687112.1:n.441G>A | ||
| ENST00000687149.1:c.269G>A | ENSP00000509745.1:p.Arg90His | |
| ENST00000687197.1:c.269G>A | ENSP00000510749.1:p.Arg90His | |
| ENST00000687235.1:n.441G>A | ||
| ENST00000687613.1:n.437G>A | ||
| ENST00000687683.1:c.269G>A | ENSP00000508522.1:p.Arg90His | |
| ENST00000688032.1:n.441G>A | ||
| ENST00000688596.1:n.441G>A | ||
| ENST00000688608.1:c.269G>A | ENSP00000508890.1:p.Arg90His | |
| ENST00000688919.1:n.422G>A | ||
| ENST00000689031.1:n.441G>A | ||
| ENST00000689717.1:n.441G>A | ||
| ENST00000689756.1:c.235+154G>A | ENSP00000509023.1:n.235+154G>A | |
| ENST00000690377.1:n.441G>A | ||
| ENST00000690678.1:c.269G>A | ENSP00000508703.1:p.Arg90His | |
| ENST00000691209.1:c.269G>A | ENSP00000510112.1:p.Arg90His | |
| ENST00000691243.1:c.269G>A | ENSP00000510654.1:p.Arg90His | |
| ENST00000692169.1:n.441G>A | ||
| ENST00000692202.1:n.437G>A | ||
| ENST00000692322.1:c.*121G>A | ENSP00000509017.1:n.*121G>A | |
| ENST00000692369.1:c.269G>A | ENSP00000508453.1:p.Arg90His | |
| ENST00000692599.1:n.441G>A | ||
| ENST00000692635.1:c.269G>A | ENSP00000508425.1:p.Arg90His | |
| ENST00000693168.1:n.441G>A | ||
| ENST00000693218.1:c.269G>A | ENSP00000510577.1:p.Arg90His | |
| ENST00000693223.1:n.913G>A | ||
| ENST00000693365.1:n.515G>A | ||
| ENST00000371984.8:c.269G>A MANE Select | ENSP00000361052.3:p.Arg90His | |
| ENST00000371984.7:c.269G>A | ENSP00000361052.3:p.Arg90His | |
| ENST00000371992.1:c.269G>A | ENSP00000361060.1:p.Arg90His | |
| ENST00000396420.7:c.269G>A | ENSP00000379698.3:p.Arg90His | |
| ENST00000489985.1:n.550G>A | ||
| ENST00000497439.5:n.393G>A | ||
| NM_001243766.1:c.269G>A | NP_001230695.1:p.Arg90His | |
| NM_001290129.1:c.203G>A | NP_001277058.1:p.Arg68His | |
| NM_001290130.1:c.-161G>A | NP_001277059.1:n.-161G>A | |
| NM_017739.3:c.269G>A | NP_060209.3:p.Arg90His | |
| XM_005271010.1:c.269G>A | XP_005271067.1:p.Arg90His | |
| XM_006710755.1:c.269G>A | XP_006710818.1:p.Arg90His | |
| XM_006710756.1:c.269G>A | XP_006710819.1:p.Arg90His | |
| XM_011541759.1:c.203G>A | XP_011540061.1:p.Arg68His | |
| XM_011541760.1:c.203G>A | XP_011540062.1:p.Arg68His | |
| XR_946706.1:n.428G>A | ||
| XM_011541760.3:c.203G>A | XP_011540062.1:p.Arg68His | |
| XM_017001690.1:c.269G>A | XP_016857179.1:p.Arg90His | |
| NM_001243766.2:c.269G>A | NP_001230695.2:p.Arg90His | |
| NM_001290129.2:c.203G>A | NP_001277058.2:p.Arg68His | |
| NM_001290130.2:c.-161G>A | NP_001277059.2:n.-161G>A | |
| NM_017739.4:c.269G>A MANE Select | NP_060209.4:p.Arg90His |