Linked Data
ClinVar Variation Id:
36479
ClinVar RCV Id:
RCV000041354
RCV000030151
RCV000057414
RCV000204379
RCV000246550
RCV000265426
RCV000350387
RCV000351657
RCV000385116
RCV000285289
RCV000290770
RCV000320485
RCV000355480
RCV000768708
RCV001028068
RCV001093839
RCV001098001
RCV001173421
RCV002496461
dbSNP Id:
rs11549668
ExAC:
1:156084760 C / T
gnomAD v2:
1-156084760-C-T
gnomAD v3:
1-156114969-C-T
gnomAD v4:
1-156114969-C-T
PubMed:
PMID:23757202
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156114969C>T , CM000663.2:g.156114969C>T | GRCh38 |
| NC_000001.10:g.156084760C>T , CM000663.1:g.156084760C>T | GRCh37 |
| NC_000001.9:g.154351384C>T | NCBI36 |
| NG_008692.2:g.37397C>T , LRG_254:g.37397C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682650.1:c.51C>T | ENSP00000506904.1:p.Ser17= | |
| ENST00000683032.1:c.51C>T | ENSP00000506771.1:p.Ser17= | |
| ENST00000684195.1:c.51C>T | ENSP00000508220.1:p.Ser17= | |
| ENST00000361308.9:c.51C>T | ENSP00000355292.6:p.Ser17= | |
| ENST00000368300.9:c.51C>T MANE Select | ENSP00000357283.4:p.Ser17= | |
| ENST00000496738.6:n.426C>T | ||
| ENST00000674518.1:c.51C>T | ENSP00000502261.1:p.Ser17= | |
| ENST00000674600.1:c.51C>T | ENSP00000501666.1:p.Ser17= | |
| ENST00000674720.1:c.51C>T | ENSP00000502798.1:p.Ser17= | |
| ENST00000675455.1:c.51C>T | ENSP00000501795.1:p.Ser17= | |
| ENST00000675667.1:c.51C>T | ENSP00000501803.1:p.Ser17= | |
| ENST00000675874.1:c.51C>T | ENSP00000501851.1:p.Ser17= | |
| ENST00000675881.1:c.51C>T | ENSP00000501670.1:p.Ser17= | |
| ENST00000675939.1:c.51C>T | ENSP00000502256.1:p.Ser17= | |
| ENST00000675989.1:n.426C>T | ||
| ENST00000676208.1:c.51C>T | ENSP00000502468.1:p.Ser17= | |
| ENST00000676283.1:n.426C>T | ||
| ENST00000676385.2:c.51C>T | ENSP00000502091.1:p.Ser17= | |
| ENST00000676434.1:c.51C>T | ENSP00000501648.1:p.Ser17= | |
| ENST00000677389.1:c.51C>T MANE Plus Clinical | ENSP00000503633.1:p.Ser17= | |
| ENST00000347559.6:c.51C>T | ENSP00000292304.3:p.Ser17= | |
| ENST00000361308.8:c.51C>T | ENSP00000355292.5:p.Ser17= | |
| ENST00000368299.7:c.51C>T | ENSP00000357282.3:p.Ser17= | |
| ENST00000368300.8:c.51C>T | ENSP00000357283.4:p.Ser17= | |
| ENST00000368301.6:c.51C>T | ENSP00000357284.2:p.Ser17= | |
| ENST00000469565.6:n.85C>T | ||
| ENST00000470199.2:n.259C>T | ||
| ENST00000478063.2:n.207C>T | ||
| ENST00000502751.5:n.329-15648C>T | ||
| NM_001282625.1:c.51C>T | NP_001269554.1:p.Ser17= | |
| NM_001282626.1:c.51C>T | NP_001269555.1:p.Ser17= | |
| NM_005572.3:c.51C>T , LRG_254t1:c.51C>T | NP_005563.1:p.Ser17= | |
| NM_170707.3:c.51C>T | NP_733821.1:p.Ser17= | |
| NM_170708.3:c.51C>T | NP_733822.1:p.Ser17= | |
| XR_921781.1:n.300C>T | ||
| XR_921781.2:n.298C>T | ||
| NM_170707.4:c.51C>T MANE Select | NP_733821.1:p.Ser17= | |
| NM_001282626.2:c.51C>T | NP_001269555.1:p.Ser17= | |
| NM_001282625.2:c.51C>T | NP_001269554.1:p.Ser17= | |
| NM_005572.4:c.51C>T MANE Plus Clinical | NP_005563.1:p.Ser17= | |
| NM_170708.4:c.51C>T | NP_733822.1:p.Ser17= |