Linked Data
ClinVar Variation Id:
448243
dbSNP Id:
rs781537575
ExAC:
11:10051321 T / A
gnomAD v2:
11-10051321-T-A
gnomAD v3:
11-10029774-T-A
gnomAD v4:
11-10029774-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.10029774T>A , CM000673.2:g.10029774T>A | GRCh38 |
| NC_000011.9:g.10051321T>A , CM000673.1:g.10051321T>A | GRCh37 |
| NC_000011.8:g.10007897T>A | NCBI36 |
| NG_008074.1:g.269434A>T , LRG_267:g.269434A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526353.2:n.654A>T | ||
| ENST00000527019.6:n.451A>T | ||
| ENST00000533661.2:n.460A>T | ||
| ENST00000533770.6:c.504A>T | ENSP00000509247.1:p.Gly168= | |
| ENST00000675281.2:c.504A>T | ENSP00000502491.1:p.Gly168= | |
| ENST00000676324.2:c.504A>T | ENSP00000502578.1:p.Gly168= | |
| ENST00000676387.2:c.504A>T | ENSP00000502779.1:p.Gly168= | |
| ENST00000685217.1:n.835A>T | ||
| ENST00000686079.1:c.504A>T | ENSP00000509599.1:p.Gly168= | |
| ENST00000687210.1:c.504A>T | ENSP00000509480.1:p.Gly168= | |
| ENST00000687256.1:c.504A>T | ENSP00000508741.1:p.Gly168= | |
| ENST00000687300.1:c.504A>T | ENSP00000508415.1:p.Gly168= | |
| ENST00000688206.1:c.504A>T | ENSP00000510516.1:p.Gly168= | |
| ENST00000688344.1:c.225A>T | ENSP00000509987.1:p.Gly75= | |
| ENST00000688417.1:n.654A>T | ||
| ENST00000689128.1:c.504A>T | ENSP00000509587.1:p.Gly168= | |
| ENST00000689258.1:c.366A>T | ENSP00000510475.1:p.Gly122= | |
| ENST00000689940.1:c.504A>T | ENSP00000508452.1:p.Gly168= | |
| ENST00000692716.1:c.504A>T | ENSP00000509545.1:p.Gly168= | |
| ENST00000693022.1:c.504A>T | ENSP00000508914.1:p.Gly168= | |
| ENST00000693201.1:c.*86A>T | ENSP00000510346.1:n.*86A>T | |
| ENST00000693212.1:c.504A>T | ENSP00000510716.1:p.Gly168= | |
| ENST00000256190.13:c.504A>T MANE Select | ENSP00000256190.8:p.Gly168= | |
| ENST00000675281.1:c.504A>T | ENSP00000502491.1:p.Gly168= | |
| ENST00000676324.1:c.504A>T | ENSP00000502578.1:p.Gly168= | |
| ENST00000676387.1:c.504A>T | ENSP00000502779.1:p.Gly168= | |
| ENST00000256190.12:c.504A>T | ENSP00000256190.8:p.Gly168= | |
| ENST00000527019.5:n.451A>T | ||
| ENST00000533661.1:n.372A>T | ||
| ENST00000533770.5:n.419A>T | ||
| ENST00000617179.4:c.363A>T | ENSP00000482806.1:p.Gly121= | |
| NM_030962.3:c.504A>T , LRG_267t1:c.504A>T | NP_112224.1:p.Gly168= | |
| XM_005253154.3:c.504A>T | XP_005253211.1:p.Gly168= | |
| XM_005253155.3:c.504A>T | XP_005253212.1:p.Gly168= | |
| XM_011520394.1:c.504A>T | XP_011518696.1:p.Gly168= | |
| XM_011520395.1:c.504A>T | XP_011518697.1:p.Gly168= | |
| XM_011520396.1:c.504A>T | XP_011518698.1:p.Gly168= | |
| XM_005253154.5:c.504A>T | XP_005253211.1:p.Gly168= | |
| XM_005253155.5:c.504A>T | XP_005253212.1:p.Gly168= | |
| XM_011520394.3:c.504A>T | XP_011518696.1:p.Gly168= | |
| XM_011520395.3:c.504A>T | XP_011518697.1:p.Gly168= | |
| XM_011520396.3:c.504A>T | XP_011518698.1:p.Gly168= | |
| XM_017018372.2:c.366A>T | XP_016873861.1:p.Gly122= | |
| XM_017018373.2:c.366A>T | XP_016873862.1:p.Gly122= | |
| XM_017018374.2:c.504A>T | XP_016873863.1:p.Gly168= | |
| XM_017018375.2:c.504A>T | XP_016873864.1:p.Gly168= | |
| XM_017018376.2:c.504A>T | XP_016873865.1:p.Gly168= | |
| XM_017018377.2:c.504A>T | XP_016873866.1:p.Gly168= | |
| XR_001747994.2:n.642A>T | ||
| NM_001386339.1:c.504A>T | NP_001373268.1:p.Gly168= | |
| NM_001386342.1:c.504A>T | NP_001373271.1:p.Gly168= | |
| NM_030962.4:c.504A>T MANE Select | NP_112224.1:p.Gly168= |