Linked Data
dbSNP Id:
rs749054978
ExAC:
1:156104151 G / A
gnomAD v2:
1-156104151-G-A
gnomAD v3:
1-156134360-G-A
gnomAD v4:
1-156134360-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156134360G>A , CM000663.2:g.156134360G>A | GRCh38 |
| NC_000001.10:g.156104151G>A , CM000663.1:g.156104151G>A | GRCh37 |
| NC_000001.9:g.154370775G>A | NCBI36 |
| NG_008692.2:g.56788G>A , LRG_254:g.56788G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.-45-43G>A | ENSP00000426535.3:n.-45-43G>A | |
| ENST00000682650.1:c.514-43G>A | ENSP00000506904.1:n.514-43G>A | |
| ENST00000683032.1:c.514-43G>A | ENSP00000506771.1:n.514-43G>A | |
| ENST00000684195.1:c.514-43G>A | ENSP00000508220.1:n.514-43G>A | |
| ENST00000361308.9:c.514-43G>A | ENSP00000355292.6:n.514-43G>A | |
| ENST00000368300.9:c.514-43G>A MANE Select | ENSP00000357283.4:n.514-43G>A | |
| ENST00000496738.6:n.889-43G>A | ||
| ENST00000504687.6:c.-151-43G>A | ENSP00000426535.2:n.-151-43G>A | |
| ENST00000674518.1:c.514-43G>A | ENSP00000502261.1:n.514-43G>A | |
| ENST00000674600.1:c.*313-43G>A | ENSP00000501666.1:n.*313-43G>A | |
| ENST00000674720.1:c.514-43G>A | ENSP00000502798.1:n.514-43G>A | |
| ENST00000675431.1:n.207-43G>A | ||
| ENST00000675455.1:c.*314-43G>A | ENSP00000501795.1:n.*314-43G>A | |
| ENST00000675667.1:c.514-43G>A | ENSP00000501803.1:n.514-43G>A | |
| ENST00000675874.1:c.357-43G>A | ENSP00000501851.1:n.357-43G>A | |
| ENST00000675881.1:c.514-43G>A | ENSP00000501670.1:n.514-43G>A | |
| ENST00000675939.1:c.514-43G>A | ENSP00000502256.1:n.514-43G>A | |
| ENST00000675989.1:n.889-43G>A | ||
| ENST00000676208.1:c.514-43G>A | ENSP00000502468.1:n.514-43G>A | |
| ENST00000676283.1:n.889-43G>A | ||
| ENST00000676385.2:c.514-43G>A | ENSP00000502091.1:n.514-43G>A | |
| ENST00000676434.1:c.514-43G>A | ENSP00000501648.1:n.514-43G>A | |
| ENST00000677389.1:c.514-43G>A MANE Plus Clinical | ENSP00000503633.1:n.514-43G>A | |
| ENST00000347559.6:c.514-43G>A | ENSP00000292304.3:n.514-43G>A | |
| ENST00000361308.8:c.514-43G>A | ENSP00000355292.5:n.514-43G>A | |
| ENST00000368297.5:c.271-43G>A | ENSP00000357280.1:n.271-43G>A | |
| ENST00000368299.7:c.514-43G>A | ENSP00000357282.3:n.514-43G>A | |
| ENST00000368300.8:c.514-43G>A | ENSP00000357283.4:n.514-43G>A | |
| ENST00000368301.6:c.514-43G>A | ENSP00000357284.2:n.514-43G>A | |
| ENST00000448611.6:c.178-43G>A | ENSP00000395597.2:n.178-43G>A | |
| ENST00000469565.6:n.548-43G>A | ||
| ENST00000470199.2:n.456-43G>A | ||
| ENST00000473598.6:c.217-43G>A | ENSP00000421821.1:n.217-43G>A | |
| ENST00000502357.5:n.412-43G>A | ||
| ENST00000502751.5:n.486-43G>A | ||
| ENST00000504687.5:c.265-43G>A | ENSP00000426535.1:n.265-43G>A | |
| ENST00000515459.5:c.*188-43G>A | ENSP00000424518.1:n.*188-43G>A | |
| NM_001257374.2:c.178-43G>A | NP_001244303.1:n.178-43G>A | |
| NM_001282624.1:c.271-43G>A | NP_001269553.1:n.271-43G>A | |
| NM_001282625.1:c.514-43G>A | NP_001269554.1:n.514-43G>A | |
| NM_001282626.1:c.514-43G>A | NP_001269555.1:n.514-43G>A | |
| NM_005572.3:c.514-43G>A , LRG_254t1:c.514-43G>A | NP_005563.1:n.514-43G>A | |
| NM_170707.3:c.514-43G>A | NP_733821.1:n.514-43G>A | |
| NM_170708.3:c.514-43G>A | NP_733822.1:n.514-43G>A | |
| XM_011509533.1:c.178-43G>A | XP_011507835.1:n.178-43G>A | |
| XM_011509534.1:c.-151-43G>A | XP_011507836.1:n.-151-43G>A | |
| XR_921781.1:n.763-43G>A | ||
| XM_011509534.2:c.-151-43G>A | XP_011507836.1:n.-151-43G>A | |
| XR_921781.2:n.761-43G>A | ||
| NM_170707.4:c.514-43G>A MANE Select | NP_733821.1:n.514-43G>A | |
| NM_001257374.3:c.178-43G>A | NP_001244303.1:n.178-43G>A | |
| NM_001282626.2:c.514-43G>A | NP_001269555.1:n.514-43G>A | |
| NM_001282624.2:c.271-43G>A | NP_001269553.1:n.271-43G>A | |
| NM_001282625.2:c.514-43G>A | NP_001269554.1:n.514-43G>A | |
| NM_005572.4:c.514-43G>A MANE Plus Clinical | NP_005563.1:n.514-43G>A | |
| NM_170708.4:c.514-43G>A | NP_733822.1:n.514-43G>A |