Linked Data
ClinVar Variation Id:
66802
ClinVar RCV Id:
RCV000057265
RCV000150953
RCV000148606
RCV000653929
RCV001172619
RCV001524022
RCV002381364
dbSNP Id:
rs150840924
ExAC:
1:156106150 C / T
gnomAD v2:
1-156106150-C-T
gnomAD v3:
1-156136359-C-T
gnomAD v4:
1-156136359-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156136359C>T , CM000663.2:g.156136359C>T | GRCh38 |
| NC_000001.10:g.156106150C>T , CM000663.1:g.156106150C>T | GRCh37 |
| NC_000001.9:g.154372774C>T | NCBI36 |
| NG_008692.2:g.58787C>T , LRG_254:g.58787C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.745C>T | ENSP00000426535.3:p.Arg249Cys | |
| ENST00000459904.2:n.67C>T | ||
| ENST00000498722.3:n.535C>T | ||
| ENST00000682650.1:c.1303C>T | ENSP00000506904.1:p.Arg435Cys | |
| ENST00000683032.1:c.1303C>T | ENSP00000506771.1:p.Arg435Cys | |
| ENST00000684195.1:c.1303C>T | ENSP00000508220.1:p.Arg435Cys | |
| ENST00000361308.9:c.1303C>T | ENSP00000355292.6:p.Arg435Cys | |
| ENST00000368300.9:c.1303C>T MANE Select | ENSP00000357283.4:p.Arg435Cys | |
| ENST00000496738.6:n.1678C>T | ||
| ENST00000674518.1:c.*653C>T | ENSP00000502261.1:n.*653C>T | |
| ENST00000674600.1:c.*1102C>T | ENSP00000501666.1:n.*1102C>T | |
| ENST00000674720.1:c.1303C>T | ENSP00000502798.1:p.Arg435Cys | |
| ENST00000675431.1:n.996C>T | ||
| ENST00000675455.1:c.*1103C>T | ENSP00000501795.1:n.*1103C>T | |
| ENST00000675667.1:c.1303C>T | ENSP00000501803.1:p.Arg435Cys | |
| ENST00000675874.1:c.*774C>T | ENSP00000501851.1:n.*774C>T | |
| ENST00000675881.1:c.*314C>T | ENSP00000501670.1:n.*314C>T | |
| ENST00000675939.1:c.1303C>T | ENSP00000502256.1:p.Arg435Cys | |
| ENST00000675989.1:n.1678C>T | ||
| ENST00000676208.1:c.*406C>T | ENSP00000502468.1:n.*406C>T | |
| ENST00000676283.1:n.1678C>T | ||
| ENST00000676385.2:c.1303C>T | ENSP00000502091.1:p.Arg435Cys | |
| ENST00000676434.1:c.*314C>T | ENSP00000501648.1:n.*314C>T | |
| ENST00000677389.1:c.1303C>T MANE Plus Clinical | ENSP00000503633.1:p.Arg435Cys | |
| ENST00000347559.6:c.1303C>T | ENSP00000292304.3:p.Arg435Cys | |
| ENST00000361308.8:c.1303C>T | ENSP00000355292.5:p.Arg435Cys | |
| ENST00000368297.5:c.1060C>T | ENSP00000357280.1:p.Arg354Cys | |
| ENST00000368298.2:n.567C>T | ||
| ENST00000368299.7:c.1303C>T | ENSP00000357282.3:p.Arg435Cys | |
| ENST00000368300.8:c.1303C>T | ENSP00000357283.4:p.Arg435Cys | |
| ENST00000368301.6:c.1303C>T | ENSP00000357284.2:p.Arg435Cys | |
| ENST00000448611.6:c.967C>T | ENSP00000395597.2:p.Arg323Cys | |
| ENST00000459904.1:n.67C>T | ||
| ENST00000473598.6:c.1006C>T | ENSP00000421821.1:p.Arg336Cys | |
| ENST00000496738.5:n.688C>T | ||
| ENST00000498722.2:n.535C>T | ||
| ENST00000508500.1:c.181C>T | ENSP00000424977.1:p.Arg61Cys | |
| NM_001257374.2:c.967C>T | NP_001244303.1:p.Arg323Cys | |
| NM_001282624.1:c.1060C>T | NP_001269553.1:p.Arg354Cys | |
| NM_001282625.1:c.1303C>T | NP_001269554.1:p.Arg435Cys | |
| NM_001282626.1:c.1303C>T | NP_001269555.1:p.Arg435Cys | |
| NM_005572.3:c.1303C>T , LRG_254t1:c.1303C>T | NP_005563.1:p.Arg435Cys | |
| NM_170707.3:c.1303C>T | NP_733821.1:p.Arg435Cys | |
| NM_170708.3:c.1303C>T | NP_733822.1:p.Arg435Cys | |
| XM_011509533.1:c.967C>T | XP_011507835.1:p.Arg323Cys | |
| XM_011509534.1:c.679C>T | XP_011507836.1:p.Arg227Cys | |
| XR_921781.1:n.1592C>T | ||
| XM_011509534.2:c.679C>T | XP_011507836.1:p.Arg227Cys | |
| XR_921781.2:n.1590C>T | ||
| NM_170707.4:c.1303C>T MANE Select | NP_733821.1:p.Arg435Cys | |
| NM_001257374.3:c.967C>T | NP_001244303.1:p.Arg323Cys | |
| NM_001282626.2:c.1303C>T | NP_001269555.1:p.Arg435Cys | |
| NM_001282624.2:c.1060C>T | NP_001269553.1:p.Arg354Cys | |
| NM_001282625.2:c.1303C>T | NP_001269554.1:p.Arg435Cys | |
| NM_005572.4:c.1303C>T MANE Plus Clinical | NP_005563.1:p.Arg435Cys | |
| NM_170708.4:c.1303C>T | NP_733822.1:p.Arg435Cys |