Linked Data
ClinVar Variation Id:
2911
dbSNP Id:
rs120074138
gnomAD v2:
11-9853837-G-A
gnomAD v4:
11-9832290-G-A
PubMed:
PMID:12687498
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9832290G>A , CM000673.2:g.9832290G>A | GRCh38 |
| NC_000011.9:g.9853837G>A , CM000673.1:g.9853837G>A | GRCh37 |
| NC_000011.8:g.9810413G>A | NCBI36 |
| NG_008074.1:g.466918C>T , LRG_267:g.466918C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530741.2:c.2290C>T | ENSP00000432643.2:p.Arg764Ter | |
| ENST00000675281.2:c.3586C>T | ENSP00000502491.1:p.Arg1196Ter | |
| ENST00000676324.2:c.3586C>T | ENSP00000502578.1:p.Arg1196Ter | |
| ENST00000676387.2:c.3472C>T | ENSP00000502779.1:p.Arg1158Ter | |
| ENST00000688344.1:c.3193C>T | ENSP00000509987.1:p.Arg1065Ter | |
| ENST00000689128.1:c.3586C>T | ENSP00000509587.1:p.Arg1196Ter | |
| ENST00000689258.1:c.3448C>T | ENSP00000510475.1:p.Arg1150Ter | |
| ENST00000689356.1:n.757C>T | ||
| ENST00000689597.1:c.2290C>T | ENSP00000510781.1:p.Arg764Ter | |
| ENST00000689674.1:c.2480C>T | ENSP00000510723.1:n.2480C>T | |
| ENST00000689940.1:c.3580C>T | ENSP00000508452.1:p.Arg1194Ter | |
| ENST00000690003.1:c.2385C>T | ENSP00000508748.1:n.2385C>T | |
| ENST00000692716.1:c.3457C>T | ENSP00000509545.1:p.Arg1153Ter | |
| ENST00000693181.1:c.2415C>T | ENSP00000510179.1:n.2415C>T | |
| ENST00000256190.13:c.3586C>T MANE Select | ENSP00000256190.8:p.Arg1196Ter | |
| ENST00000675281.1:c.3586C>T | ENSP00000502491.1:p.Arg1196Ter | |
| ENST00000676324.1:c.3586C>T | ENSP00000502578.1:p.Arg1196Ter | |
| ENST00000676387.1:c.3472C>T | ENSP00000502779.1:p.Arg1158Ter | |
| ENST00000256190.12:c.3586C>T | ENSP00000256190.8:p.Arg1196Ter | |
| ENST00000530741.1:c.237C>T | ||
| ENST00000617179.4:c.3445C>T | ENSP00000482806.1:p.Arg1149Ter | |
| NM_030962.3:c.3586C>T , LRG_267t1:c.3586C>T | NP_112224.1:p.Arg1196Ter | |
| XM_005253154.3:c.3586C>T | XP_005253211.1:p.Arg1196Ter | |
| XM_005253155.3:c.3457C>T | XP_005253212.1:p.Arg1153Ter | |
| XM_011520394.1:c.3472C>T | XP_011518696.1:p.Arg1158Ter | |
| XM_011520395.1:c.3586C>T | XP_011518697.1:p.Arg1196Ter | |
| XM_005253154.5:c.3586C>T | XP_005253211.1:p.Arg1196Ter | |
| XM_005253155.5:c.3457C>T | XP_005253212.1:p.Arg1153Ter | |
| XM_011520394.3:c.3472C>T | XP_011518696.1:p.Arg1158Ter | |
| XM_011520395.3:c.3586C>T | XP_011518697.1:p.Arg1196Ter | |
| XM_017018372.2:c.3448C>T | XP_016873861.1:p.Arg1150Ter | |
| XM_017018373.2:c.3448C>T | XP_016873862.1:p.Arg1150Ter | |
| XM_017018374.2:c.3457C>T | XP_016873863.1:p.Arg1153Ter | |
| XM_017018375.2:c.3586C>T | XP_016873864.1:p.Arg1196Ter | |
| XM_017018376.2:c.3586C>T | XP_016873865.1:p.Arg1196Ter | |
| XR_001747994.2:n.3724C>T | ||
| NM_001386339.1:c.3586C>T | NP_001373268.1:p.Arg1196Ter | |
| NM_001386342.1:c.3457C>T | NP_001373271.1:p.Arg1153Ter | |
| NM_030962.4:c.3586C>T MANE Select | NP_112224.1:p.Arg1196Ter |