Linked Data
ClinVar Variation Id:
48062
ClinVar RCV Id:
RCV000041345
RCV000057395
RCV000211467
RCV000148598
RCV000249770
RCV000768710
RCV001081311
RCV001096444
RCV001096445
RCV001096446
RCV001096447
RCV001101878
RCV001101879
RCV001101881
RCV001173420
RCV001096443
RCV001101880
RCV004528231
dbSNP Id:
rs41313880
ExAC:
1:156100408 C / T
gnomAD v2:
1-156100408-C-T
gnomAD v3:
1-156130617-C-T
gnomAD v4:
1-156130617-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156130617C>T , CM000663.2:g.156130617C>T | GRCh38 |
| NC_000001.10:g.156100408C>T , CM000663.1:g.156100408C>T | GRCh37 |
| NC_000001.9:g.154367032C>T | NCBI36 |
| NG_008692.2:g.53045C>T , LRG_254:g.53045C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504687.7:c.-202C>T | ENSP00000426535.3:n.-202C>T | |
| ENST00000682650.1:c.357C>T | ENSP00000506904.1:p.Arg119= | |
| ENST00000683032.1:c.357C>T | ENSP00000506771.1:p.Arg119= | |
| ENST00000684195.1:c.357C>T | ENSP00000508220.1:p.Arg119= | |
| ENST00000361308.9:c.357C>T | ENSP00000355292.6:p.Arg119= | |
| ENST00000368300.9:c.357C>T MANE Select | ENSP00000357283.4:p.Arg119= | |
| ENST00000496738.6:n.732C>T | ||
| ENST00000504687.6:c.-308C>T | ENSP00000426535.2:n.-308C>T | |
| ENST00000674518.1:c.357C>T | ENSP00000502261.1:p.Arg119= | |
| ENST00000674600.1:c.*156C>T | ENSP00000501666.1:n.*156C>T | |
| ENST00000674720.1:c.357C>T | ENSP00000502798.1:p.Arg119= | |
| ENST00000675431.1:n.50C>T | ||
| ENST00000675455.1:c.*157C>T | ENSP00000501795.1:n.*157C>T | |
| ENST00000675667.1:c.357C>T | ENSP00000501803.1:p.Arg119= | |
| ENST00000675874.1:c.357-3786C>T | ENSP00000501851.1:n.357-3786C>T | |
| ENST00000675881.1:c.357C>T | ENSP00000501670.1:p.Arg119= | |
| ENST00000675939.1:c.357C>T | ENSP00000502256.1:p.Arg119= | |
| ENST00000675989.1:n.732C>T | ||
| ENST00000676208.1:c.357C>T | ENSP00000502468.1:p.Arg119= | |
| ENST00000676283.1:n.732C>T | ||
| ENST00000676385.2:c.357C>T | ENSP00000502091.1:p.Arg119= | |
| ENST00000676434.1:c.357C>T | ENSP00000501648.1:p.Arg119= | |
| ENST00000677389.1:c.357C>T MANE Plus Clinical | ENSP00000503633.1:p.Arg119= | |
| ENST00000347559.6:c.357C>T | ENSP00000292304.3:p.Arg119= | |
| ENST00000361308.8:c.357C>T | ENSP00000355292.5:p.Arg119= | |
| ENST00000368297.5:c.114C>T | ENSP00000357280.1:p.Leu38= | |
| ENST00000368299.7:c.357C>T | ENSP00000357282.3:p.Arg119= | |
| ENST00000368300.8:c.357C>T | ENSP00000357283.4:p.Arg119= | |
| ENST00000368301.6:c.357C>T | ENSP00000357284.2:p.Arg119= | |
| ENST00000448611.6:c.21C>T | ENSP00000395597.2:p.Cys7= | |
| ENST00000469565.6:n.391C>T | ||
| ENST00000470199.2:n.357-58C>T | ||
| ENST00000473598.6:c.60C>T | ENSP00000421821.1:p.Gly20= | |
| ENST00000502357.5:n.255C>T | ||
| ENST00000502751.5:n.329C>T | ||
| ENST00000504687.5:c.108C>T | ENSP00000426535.1:p.Phe36= | |
| ENST00000515459.5:c.*31C>T | ENSP00000424518.1:n.*31C>T | |
| NM_001257374.2:c.21C>T | NP_001244303.1:p.Cys7= | |
| NM_001282624.1:c.114C>T | NP_001269553.1:p.Leu38= | |
| NM_001282625.1:c.357C>T | NP_001269554.1:p.Arg119= | |
| NM_001282626.1:c.357C>T | NP_001269555.1:p.Arg119= | |
| NM_005572.3:c.357C>T , LRG_254t1:c.357C>T | NP_005563.1:p.Arg119= | |
| NM_170707.3:c.357C>T | NP_733821.1:p.Arg119= | |
| NM_170708.3:c.357C>T | NP_733822.1:p.Arg119= | |
| XM_011509533.1:c.21C>T | XP_011507835.1:p.Cys7= | |
| XM_011509534.1:c.-308C>T | XP_011507836.1:n.-308C>T | |
| XR_921781.1:n.606C>T | ||
| XM_011509534.2:c.-308C>T | XP_011507836.1:n.-308C>T | |
| XR_921781.2:n.604C>T | ||
| NM_170707.4:c.357C>T MANE Select | NP_733821.1:p.Arg119= | |
| NM_001257374.3:c.21C>T | NP_001244303.1:p.Cys7= | |
| NM_001282626.2:c.357C>T | NP_001269555.1:p.Arg119= | |
| NM_001282624.2:c.114C>T | NP_001269553.1:p.Leu38= | |
| NM_001282625.2:c.357C>T | NP_001269554.1:p.Arg119= | |
| NM_005572.4:c.357C>T MANE Plus Clinical | NP_005563.1:p.Arg119= | |
| NM_170708.4:c.357C>T | NP_733822.1:p.Arg119= |