Linked Data
ClinVar Variation Id:
448234
dbSNP Id:
rs959559753
gnomAD v2:
11-10014540-G-A
gnomAD v3:
11-9992993-G-A
gnomAD v4:
11-9992993-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9992993G>A , CM000673.2:g.9992993G>A | GRCh38 |
| NC_000011.9:g.10014540G>A , CM000673.1:g.10014540G>A | GRCh37 |
| NC_000011.8:g.9971116G>A | NCBI36 |
| NG_008074.1:g.306215C>T , LRG_267:g.306215C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526353.2:n.1314C>T | ||
| ENST00000533770.6:c.1164C>T | ENSP00000509247.1:p.His388= | |
| ENST00000675281.2:c.1164C>T | ENSP00000502491.1:p.His388= | |
| ENST00000676324.2:c.1164C>T | ENSP00000502578.1:p.His388= | |
| ENST00000676387.2:c.1050C>T | ENSP00000502779.1:p.His350= | |
| ENST00000687210.1:c.1164C>T | ENSP00000509480.1:p.His388= | |
| ENST00000688344.1:c.771C>T | ENSP00000509987.1:p.His257= | |
| ENST00000688417.1:n.1314C>T | ||
| ENST00000689128.1:c.1164C>T | ENSP00000509587.1:p.His388= | |
| ENST00000689258.1:c.1026C>T | ENSP00000510475.1:p.His342= | |
| ENST00000689940.1:c.1164C>T | ENSP00000508452.1:p.His388= | |
| ENST00000692716.1:c.1164C>T | ENSP00000509545.1:p.His388= | |
| ENST00000256190.13:c.1164C>T MANE Select | ENSP00000256190.8:p.His388= | |
| ENST00000675281.1:c.1164C>T | ENSP00000502491.1:p.His388= | |
| ENST00000676324.1:c.1164C>T | ENSP00000502578.1:p.His388= | |
| ENST00000676387.1:c.1050C>T | ENSP00000502779.1:p.His350= | |
| ENST00000256190.12:c.1164C>T | ENSP00000256190.8:p.His388= | |
| ENST00000420722.2:c.112C>T | ||
| ENST00000533770.5:n.1079C>T | ||
| ENST00000617179.4:c.1023C>T | ENSP00000482806.1:p.His341= | |
| NM_030962.3:c.1164C>T , LRG_267t1:c.1164C>T | NP_112224.1:p.His388= | |
| XM_005253154.3:c.1164C>T | XP_005253211.1:p.His388= | |
| XM_005253155.3:c.1164C>T | XP_005253212.1:p.His388= | |
| XM_011520394.1:c.1050C>T | XP_011518696.1:p.His350= | |
| XM_011520395.1:c.1164C>T | XP_011518697.1:p.His388= | |
| XM_011520396.1:c.1164C>T | XP_011518698.1:p.His388= | |
| XM_005253154.5:c.1164C>T | XP_005253211.1:p.His388= | |
| XM_005253155.5:c.1164C>T | XP_005253212.1:p.His388= | |
| XM_011520394.3:c.1050C>T | XP_011518696.1:p.His350= | |
| XM_011520395.3:c.1164C>T | XP_011518697.1:p.His388= | |
| XM_011520396.3:c.1164C>T | XP_011518698.1:p.His388= | |
| XM_017018372.2:c.1026C>T | XP_016873861.1:p.His342= | |
| XM_017018373.2:c.1026C>T | XP_016873862.1:p.His342= | |
| XM_017018374.2:c.1164C>T | XP_016873863.1:p.His388= | |
| XM_017018375.2:c.1164C>T | XP_016873864.1:p.His388= | |
| XM_017018376.2:c.1164C>T | XP_016873865.1:p.His388= | |
| XM_017018377.2:c.1164C>T | XP_016873866.1:p.His388= | |
| XR_001747994.2:n.1302C>T | ||
| NM_001386339.1:c.1164C>T | NP_001373268.1:p.His388= | |
| NM_001386342.1:c.1164C>T | NP_001373271.1:p.His388= | |
| NM_030962.4:c.1164C>T MANE Select | NP_112224.1:p.His388= |