Linked Data
ClinVar Variation Id:
543491
dbSNP Id:
rs120074139
gnomAD v3:
11-9968482-G-T
gnomAD v4:
11-9968482-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9968482G>T , CM000673.2:g.9968482G>T | GRCh38 |
| NC_000011.9:g.9990029G>T , CM000673.1:g.9990029G>T | GRCh37 |
| NC_000011.8:g.9946605G>T | NCBI36 |
| NG_008074.1:g.330726C>A , LRG_267:g.330726C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000420722.3:c.163C>A | ENSP00000410478.3:p.Arg55= | |
| ENST00000526353.2:n.1609C>A | ||
| ENST00000530741.2:c.163C>A | ENSP00000432643.2:p.Arg55= | |
| ENST00000533770.6:c.1459C>A | ENSP00000509247.1:p.Arg487= | |
| ENST00000675281.2:c.1459C>A | ENSP00000502491.1:p.Arg487= | |
| ENST00000676324.2:c.1459C>A | ENSP00000502578.1:p.Arg487= | |
| ENST00000676387.2:c.1345C>A | ENSP00000502779.1:p.Arg449= | |
| ENST00000687210.1:c.*81C>A | ENSP00000509480.1:n.*81C>A | |
| ENST00000688344.1:c.1066C>A | ENSP00000509987.1:p.Arg356= | |
| ENST00000688417.1:n.1609C>A | ||
| ENST00000689128.1:c.1459C>A | ENSP00000509587.1:p.Arg487= | |
| ENST00000689258.1:c.1321C>A | ENSP00000510475.1:p.Arg441= | |
| ENST00000689597.1:c.163C>A | ENSP00000510781.1:p.Arg55= | |
| ENST00000689674.1:c.163C>A | ENSP00000510723.1:p.Arg55= | |
| ENST00000689940.1:c.1459C>A | ENSP00000508452.1:p.Arg487= | |
| ENST00000690003.1:c.163C>A | ENSP00000508748.1:p.Arg55= | |
| ENST00000690234.1:c.167C>A | ENSP00000510288.1:p.Ala56Glu | |
| ENST00000692716.1:c.1330C>A | ENSP00000509545.1:p.Arg444= | |
| ENST00000693181.1:c.163C>A | ENSP00000510179.1:p.Arg55= | |
| ENST00000256190.13:c.1459C>A MANE Select | ENSP00000256190.8:p.Arg487= | |
| ENST00000675281.1:c.1459C>A | ENSP00000502491.1:p.Arg487= | |
| ENST00000676324.1:c.1459C>A | ENSP00000502578.1:p.Arg487= | |
| ENST00000676387.1:c.1345C>A | ENSP00000502779.1:p.Arg449= | |
| ENST00000256190.12:c.1459C>A | ENSP00000256190.8:p.Arg487= | |
| ENST00000420722.2:c.278C>A | ||
| ENST00000533770.5:n.1374C>A | ||
| ENST00000617179.4:c.1318C>A | ENSP00000482806.1:p.Arg440= | |
| NM_030962.3:c.1459C>A , LRG_267t1:c.1459C>A | NP_112224.1:p.Arg487= | |
| XM_005253154.3:c.1459C>A | XP_005253211.1:p.Arg487= | |
| XM_005253155.3:c.1330C>A | XP_005253212.1:p.Arg444= | |
| XM_011520394.1:c.1345C>A | XP_011518696.1:p.Arg449= | |
| XM_011520395.1:c.1459C>A | XP_011518697.1:p.Arg487= | |
| XM_011520396.1:c.1459C>A | XP_011518698.1:p.Arg487= | |
| XM_005253154.5:c.1459C>A | XP_005253211.1:p.Arg487= | |
| XM_005253155.5:c.1330C>A | XP_005253212.1:p.Arg444= | |
| XM_011520394.3:c.1345C>A | XP_011518696.1:p.Arg449= | |
| XM_011520395.3:c.1459C>A | XP_011518697.1:p.Arg487= | |
| XM_011520396.3:c.1459C>A | XP_011518698.1:p.Arg487= | |
| XM_017018372.2:c.1321C>A | XP_016873861.1:p.Arg441= | |
| XM_017018373.2:c.1321C>A | XP_016873862.1:p.Arg441= | |
| XM_017018374.2:c.1330C>A | XP_016873863.1:p.Arg444= | |
| XM_017018375.2:c.1459C>A | XP_016873864.1:p.Arg487= | |
| XM_017018376.2:c.1459C>A | XP_016873865.1:p.Arg487= | |
| XM_017018377.2:c.1459C>A | XP_016873866.1:p.Arg487= | |
| XR_001747994.2:n.1597C>A | ||
| NM_001386339.1:c.1459C>A | NP_001373268.1:p.Arg487= | |
| NM_001386342.1:c.1330C>A | NP_001373271.1:p.Arg444= | |
| NM_030962.4:c.1459C>A MANE Select | NP_112224.1:p.Arg487= |