Linked Data
ClinVar Variation Id:
66959
dbSNP Id:
rs267607681
gnomAD v2:
1-156105685-C-G
gnomAD v3:
1-156135894-C-G
gnomAD v4:
1-156135894-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156135894C>G , CM000663.2:g.156135894C>G | GRCh38 |
| NC_000001.10:g.156105685C>G , CM000663.1:g.156105685C>G | GRCh37 |
| NC_000001.9:g.154372309C>G | NCBI36 |
| NG_008692.2:g.58322C>G , LRG_254:g.58322C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.379-7C>G | ENSP00000426535.3:n.379-7C>G | |
| ENST00000498722.3:n.162C>G | ||
| ENST00000682650.1:c.937-7C>G | ENSP00000506904.1:n.937-7C>G | |
| ENST00000683032.1:c.937-7C>G | ENSP00000506771.1:n.937-7C>G | |
| ENST00000684195.1:c.937-7C>G | ENSP00000508220.1:n.937-7C>G | |
| ENST00000361308.9:c.937-7C>G | ENSP00000355292.6:n.937-7C>G | |
| ENST00000368300.9:c.937-7C>G MANE Select | ENSP00000357283.4:n.937-7C>G | |
| ENST00000496738.6:n.1312-7C>G | ||
| ENST00000674518.1:c.*287-7C>G | ENSP00000502261.1:n.*287-7C>G | |
| ENST00000674600.1:c.*736-7C>G | ENSP00000501666.1:n.*736-7C>G | |
| ENST00000674720.1:c.937-7C>G | ENSP00000502798.1:n.937-7C>G | |
| ENST00000675431.1:n.630-7C>G | ||
| ENST00000675455.1:c.*737-7C>G | ENSP00000501795.1:n.*737-7C>G | |
| ENST00000675667.1:c.937-7C>G | ENSP00000501803.1:n.937-7C>G | |
| ENST00000675874.1:c.*408-7C>G | ENSP00000501851.1:n.*408-7C>G | |
| ENST00000675881.1:c.970C>G | ENSP00000501670.1:p.Pro324Ala | |
| ENST00000675939.1:c.937-7C>G | ENSP00000502256.1:n.937-7C>G | |
| ENST00000675989.1:n.1312-7C>G | ||
| ENST00000676208.1:c.970C>G | ENSP00000502468.1:p.Pro324Ala | |
| ENST00000676283.1:n.1312-7C>G | ||
| ENST00000676385.2:c.937-7C>G | ENSP00000502091.1:n.937-7C>G | |
| ENST00000676434.1:c.970C>G | ENSP00000501648.1:p.Pro324Ala | |
| ENST00000677389.1:c.937-7C>G MANE Plus Clinical | ENSP00000503633.1:n.937-7C>G | |
| ENST00000347559.6:c.937-7C>G | ENSP00000292304.3:n.937-7C>G | |
| ENST00000361308.8:c.937-7C>G | ENSP00000355292.5:n.937-7C>G | |
| ENST00000368297.5:c.694-7C>G | ENSP00000357280.1:n.694-7C>G | |
| ENST00000368298.2:n.201-7C>G | ||
| ENST00000368299.7:c.937-7C>G | ENSP00000357282.3:n.937-7C>G | |
| ENST00000368300.8:c.937-7C>G | ENSP00000357283.4:n.937-7C>G | |
| ENST00000368301.6:c.937-7C>G | ENSP00000357284.2:n.937-7C>G | |
| ENST00000448611.6:c.601-7C>G | ENSP00000395597.2:n.601-7C>G | |
| ENST00000473598.6:c.640-7C>G | ENSP00000421821.1:n.640-7C>G | |
| ENST00000496738.5:n.315C>G | ||
| ENST00000498722.2:n.162C>G | ||
| NM_001257374.2:c.601-7C>G | NP_001244303.1:n.601-7C>G | |
| NM_001282624.1:c.694-7C>G | NP_001269553.1:n.694-7C>G | |
| NM_001282625.1:c.937-7C>G | NP_001269554.1:n.937-7C>G | |
| NM_001282626.1:c.937-7C>G | NP_001269555.1:n.937-7C>G | |
| NM_005572.3:c.937-7C>G , LRG_254t1:c.937-7C>G | NP_005563.1:n.937-7C>G | |
| NM_170707.3:c.937-7C>G | NP_733821.1:n.937-7C>G | |
| NM_170708.3:c.937-7C>G | NP_733822.1:n.937-7C>G | |
| XM_011509533.1:c.601-7C>G | XP_011507835.1:n.601-7C>G | |
| XM_011509534.1:c.306C>G | XP_011507836.1:p.Pro102= | |
| XR_921781.1:n.1219C>G | ||
| XM_011509534.2:c.306C>G | XP_011507836.1:p.Pro102= | |
| XR_921781.2:n.1217C>G | ||
| NM_170707.4:c.937-7C>G MANE Select | NP_733821.1:n.937-7C>G | |
| NM_001257374.3:c.601-7C>G | NP_001244303.1:n.601-7C>G | |
| NM_001282626.2:c.937-7C>G | NP_001269555.1:n.937-7C>G | |
| NM_001282624.2:c.694-7C>G | NP_001269553.1:n.694-7C>G | |
| NM_001282625.2:c.937-7C>G | NP_001269554.1:n.937-7C>G | |
| NM_005572.4:c.937-7C>G MANE Plus Clinical | NP_005563.1:n.937-7C>G | |
| NM_170708.4:c.937-7C>G | NP_733822.1:n.937-7C>G |