Linked Data
ClinVar Variation Id:
200927
dbSNP Id:
rs374768416
gnomAD v2:
1-156105918-C-G
gnomAD v3:
1-156136127-C-G
gnomAD v4:
1-156136127-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156136127C>G , CM000663.2:g.156136127C>G | GRCh38 |
| NC_000001.10:g.156105918C>G , CM000663.1:g.156105918C>G | GRCh37 |
| NC_000001.9:g.154372542C>G | NCBI36 |
| NG_008692.2:g.58555C>G , LRG_254:g.58555C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.599+6C>G | ENSP00000426535.3:n.599+6C>G | |
| ENST00000498722.3:n.389+6C>G | ||
| ENST00000682650.1:c.1157+6C>G | ENSP00000506904.1:n.1157+6C>G | |
| ENST00000683032.1:c.1157+6C>G | ENSP00000506771.1:n.1157+6C>G | |
| ENST00000684195.1:c.1157+6C>G | ENSP00000508220.1:n.1157+6C>G | |
| ENST00000361308.9:c.1157+6C>G | ENSP00000355292.6:n.1157+6C>G | |
| ENST00000368300.9:c.1157+6C>G MANE Select | ENSP00000357283.4:n.1157+6C>G | |
| ENST00000496738.6:n.1532+6C>G | ||
| ENST00000674518.1:c.*507+6C>G | ENSP00000502261.1:n.*507+6C>G | |
| ENST00000674600.1:c.*956+6C>G | ENSP00000501666.1:n.*956+6C>G | |
| ENST00000674720.1:c.1157+6C>G | ENSP00000502798.1:n.1157+6C>G | |
| ENST00000675431.1:n.850+6C>G | ||
| ENST00000675455.1:c.*957+6C>G | ENSP00000501795.1:n.*957+6C>G | |
| ENST00000675667.1:c.1157+6C>G | ENSP00000501803.1:n.1157+6C>G | |
| ENST00000675874.1:c.*628+6C>G | ENSP00000501851.1:n.*628+6C>G | |
| ENST00000675881.1:c.*168+6C>G | ENSP00000501670.1:n.*168+6C>G | |
| ENST00000675939.1:c.1157+6C>G | ENSP00000502256.1:n.1157+6C>G | |
| ENST00000675989.1:n.1532+6C>G | ||
| ENST00000676208.1:c.*174C>G | ENSP00000502468.1:n.*174C>G | |
| ENST00000676283.1:n.1532+6C>G | ||
| ENST00000676385.2:c.1157+6C>G | ENSP00000502091.1:n.1157+6C>G | |
| ENST00000676434.1:c.*168+6C>G | ENSP00000501648.1:n.*168+6C>G | |
| ENST00000677389.1:c.1157+6C>G MANE Plus Clinical | ENSP00000503633.1:n.1157+6C>G | |
| ENST00000347559.6:c.1157+6C>G | ENSP00000292304.3:n.1157+6C>G | |
| ENST00000361308.8:c.1157+6C>G | ENSP00000355292.5:n.1157+6C>G | |
| ENST00000368297.5:c.914+6C>G | ENSP00000357280.1:n.914+6C>G | |
| ENST00000368298.2:n.421+6C>G | ||
| ENST00000368299.7:c.1157+6C>G | ENSP00000357282.3:n.1157+6C>G | |
| ENST00000368300.8:c.1157+6C>G | ENSP00000357283.4:n.1157+6C>G | |
| ENST00000368301.6:c.1157+6C>G | ENSP00000357284.2:n.1157+6C>G | |
| ENST00000448611.6:c.821+6C>G | ENSP00000395597.2:n.821+6C>G | |
| ENST00000473598.6:c.860+6C>G | ENSP00000421821.1:n.860+6C>G | |
| ENST00000496738.5:n.542+6C>G | ||
| ENST00000498722.2:n.389+6C>G | ||
| ENST00000508500.1:c.35+6C>G | ENSP00000424977.1:n.35+6C>G | |
| NM_001257374.2:c.821+6C>G | NP_001244303.1:n.821+6C>G | |
| NM_001282624.1:c.914+6C>G | NP_001269553.1:n.914+6C>G | |
| NM_001282625.1:c.1157+6C>G | NP_001269554.1:n.1157+6C>G | |
| NM_001282626.1:c.1157+6C>G | NP_001269555.1:n.1157+6C>G | |
| NM_005572.3:c.1157+6C>G , LRG_254t1:c.1157+6C>G | NP_005563.1:n.1157+6C>G | |
| NM_170707.3:c.1157+6C>G | NP_733821.1:n.1157+6C>G | |
| NM_170708.3:c.1157+6C>G | NP_733822.1:n.1157+6C>G | |
| XM_011509533.1:c.821+6C>G | XP_011507835.1:n.821+6C>G | |
| XM_011509534.1:c.533+6C>G | XP_011507836.1:n.533+6C>G | |
| XR_921781.1:n.1446+6C>G | ||
| XM_011509534.2:c.533+6C>G | XP_011507836.1:n.533+6C>G | |
| XR_921781.2:n.1444+6C>G | ||
| NM_170707.4:c.1157+6C>G MANE Select | NP_733821.1:n.1157+6C>G | |
| NM_001257374.3:c.821+6C>G | NP_001244303.1:n.821+6C>G | |
| NM_001282626.2:c.1157+6C>G | NP_001269555.1:n.1157+6C>G | |
| NM_001282624.2:c.914+6C>G | NP_001269553.1:n.914+6C>G | |
| NM_001282625.2:c.1157+6C>G | NP_001269554.1:n.1157+6C>G | |
| NM_005572.4:c.1157+6C>G MANE Plus Clinical | NP_005563.1:n.1157+6C>G | |
| NM_170708.4:c.1157+6C>G | NP_733822.1:n.1157+6C>G |