Linked Data
ClinVar Variation Id:
1522462
ClinVar RCV Id:
RCV002034441
dbSNP Id:
rs1651695560
gnomAD v4:
1-156136964-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156136964A>G , CM000663.2:g.156136964A>G | GRCh38 |
| NC_000001.10:g.156106755A>G , CM000663.1:g.156106755A>G | GRCh37 |
| NC_000001.9:g.154373379A>G | NCBI36 |
| NG_008692.2:g.59392A>G , LRG_254:g.59392A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.866A>G | ENSP00000426535.3:p.Asp289Gly | |
| ENST00000459904.2:n.672A>G | ||
| ENST00000498722.3:n.656A>G | ||
| ENST00000682650.1:c.1424A>G | ENSP00000506904.1:p.Asp475Gly | |
| ENST00000683032.1:c.1424A>G | ENSP00000506771.1:p.Asp475Gly | |
| ENST00000684195.1:c.1424A>G | ENSP00000508220.1:p.Asp475Gly | |
| ENST00000361308.9:c.1424A>G | ENSP00000355292.6:p.Asp475Gly | |
| ENST00000368300.9:c.1424A>G MANE Select | ENSP00000357283.4:p.Asp475Gly | |
| ENST00000496738.6:n.1799A>G | ||
| ENST00000674518.1:c.*774A>G | ENSP00000502261.1:n.*774A>G | |
| ENST00000674600.1:c.*1223A>G | ENSP00000501666.1:n.*1223A>G | |
| ENST00000674720.1:c.1537A>G | ENSP00000502798.1:p.Met513Val | |
| ENST00000675431.1:n.1117A>G | ||
| ENST00000675455.1:c.*1224A>G | ENSP00000501795.1:n.*1224A>G | |
| ENST00000675667.1:c.1424A>G | ENSP00000501803.1:p.Asp475Gly | |
| ENST00000675874.1:c.*895A>G | ENSP00000501851.1:n.*895A>G | |
| ENST00000675881.1:c.*435A>G | ENSP00000501670.1:n.*435A>G | |
| ENST00000675939.1:c.1424A>G | ENSP00000502256.1:p.Asp475Gly | |
| ENST00000675989.1:n.2283A>G | ||
| ENST00000676208.1:c.*527A>G | ENSP00000502468.1:n.*527A>G | |
| ENST00000676283.1:n.1799A>G | ||
| ENST00000676385.2:c.1424A>G | ENSP00000502091.1:p.Asp475Gly | |
| ENST00000676434.1:c.*435A>G | ENSP00000501648.1:n.*435A>G | |
| ENST00000677389.1:c.1424A>G MANE Plus Clinical | ENSP00000503633.1:p.Asp475Gly | |
| ENST00000347559.6:c.1424A>G | ENSP00000292304.3:p.Asp475Gly | |
| ENST00000361308.8:c.1312-227A>G | ENSP00000355292.5:n.1312-227A>G | |
| ENST00000368297.5:c.1181A>G | ENSP00000357280.1:p.Asp394Gly | |
| ENST00000368298.2:n.1172A>G | ||
| ENST00000368299.7:c.1424A>G | ENSP00000357282.3:p.Asp475Gly | |
| ENST00000368300.8:c.1424A>G | ENSP00000357283.4:p.Asp475Gly | |
| ENST00000368301.6:c.1424A>G | ENSP00000357284.2:p.Asp475Gly | |
| ENST00000448611.6:c.1088A>G | ENSP00000395597.2:p.Asp363Gly | |
| ENST00000459904.1:n.672A>G | ||
| ENST00000473598.6:c.1127A>G | ENSP00000421821.1:p.Asp376Gly | |
| ENST00000496738.5:n.809A>G | ||
| ENST00000498722.2:n.656A>G | ||
| ENST00000508500.1:c.302A>G | ENSP00000424977.1:p.Asp101Gly | |
| NM_001257374.2:c.1088A>G | NP_001244303.1:p.Asp363Gly | |
| NM_001282624.1:c.1181A>G | NP_001269553.1:p.Asp394Gly | |
| NM_001282625.1:c.1424A>G | NP_001269554.1:p.Asp475Gly | |
| NM_001282626.1:c.1424A>G | NP_001269555.1:p.Asp475Gly | |
| NM_005572.3:c.1424A>G , LRG_254t1:c.1424A>G | NP_005563.1:p.Asp475Gly | |
| NM_170707.3:c.1424A>G | NP_733821.1:p.Asp475Gly | |
| NM_170708.3:c.1424A>G | NP_733822.1:p.Asp475Gly | |
| XM_011509533.1:c.1088A>G | XP_011507835.1:p.Asp363Gly | |
| XM_011509534.1:c.800A>G | XP_011507836.1:p.Asp267Gly | |
| XR_921781.1:n.1713A>G | ||
| XM_011509534.2:c.800A>G | XP_011507836.1:p.Asp267Gly | |
| XR_921781.2:n.1711A>G | ||
| NM_170707.4:c.1424A>G MANE Select | NP_733821.1:p.Asp475Gly | |
| NM_001257374.3:c.1088A>G | NP_001244303.1:p.Asp363Gly | |
| NM_001282626.2:c.1424A>G | NP_001269555.1:p.Asp475Gly | |
| NM_001282624.2:c.1181A>G | NP_001269553.1:p.Asp394Gly | |
| NM_001282625.2:c.1424A>G | NP_001269554.1:p.Asp475Gly | |
| NM_005572.4:c.1424A>G MANE Plus Clinical | NP_005563.1:p.Asp475Gly | |
| NM_170708.4:c.1424A>G | NP_733822.1:p.Asp475Gly |