Linked Data
ClinVar Variation Id:
378088
ClinVar RCV Id:
RCV000422715
RCV000768707
RCV001173407
RCV002488882
RCV003995962
RCV000527270
RCV002379298
dbSNP Id:
rs369823958
gnomAD v2:
1-156084721-G-A
gnomAD v3:
1-156114930-G-A
gnomAD v4:
1-156114930-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156114930G>A , CM000663.2:g.156114930G>A | GRCh38 |
| NC_000001.10:g.156084721G>A , CM000663.1:g.156084721G>A | GRCh37 |
| NC_000001.9:g.154351345G>A | NCBI36 |
| NG_008692.2:g.37358G>A , LRG_254:g.37358G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682650.1:c.12G>A | ENSP00000506904.1:p.Pro4= | |
| ENST00000683032.1:c.12G>A | ENSP00000506771.1:p.Pro4= | |
| ENST00000684195.1:c.12G>A | ENSP00000508220.1:p.Pro4= | |
| ENST00000361308.9:c.12G>A | ENSP00000355292.6:p.Pro4= | |
| ENST00000368300.9:c.12G>A MANE Select | ENSP00000357283.4:p.Pro4= | |
| ENST00000496738.6:n.387G>A | ||
| ENST00000674518.1:c.12G>A | ENSP00000502261.1:p.Pro4= | |
| ENST00000674600.1:c.12G>A | ENSP00000501666.1:p.Pro4= | |
| ENST00000674720.1:c.12G>A | ENSP00000502798.1:p.Pro4= | |
| ENST00000675455.1:c.12G>A | ENSP00000501795.1:p.Pro4= | |
| ENST00000675667.1:c.12G>A | ENSP00000501803.1:p.Pro4= | |
| ENST00000675874.1:c.12G>A | ENSP00000501851.1:p.Pro4= | |
| ENST00000675881.1:c.12G>A | ENSP00000501670.1:p.Pro4= | |
| ENST00000675939.1:c.12G>A | ENSP00000502256.1:p.Pro4= | |
| ENST00000675989.1:n.387G>A | ||
| ENST00000676208.1:c.12G>A | ENSP00000502468.1:p.Pro4= | |
| ENST00000676283.1:n.387G>A | ||
| ENST00000676385.2:c.12G>A | ENSP00000502091.1:p.Pro4= | |
| ENST00000676434.1:c.12G>A | ENSP00000501648.1:p.Pro4= | |
| ENST00000677389.1:c.12G>A MANE Plus Clinical | ENSP00000503633.1:p.Pro4= | |
| ENST00000347559.6:c.12G>A | ENSP00000292304.3:p.Pro4= | |
| ENST00000361308.8:c.12G>A | ENSP00000355292.5:p.Pro4= | |
| ENST00000368299.7:c.12G>A | ENSP00000357282.3:p.Pro4= | |
| ENST00000368300.8:c.12G>A | ENSP00000357283.4:p.Pro4= | |
| ENST00000368301.6:c.12G>A | ENSP00000357284.2:p.Pro4= | |
| ENST00000469565.6:n.80-34G>A | ||
| ENST00000470199.2:n.220G>A | ||
| ENST00000478063.2:n.201+19G>A | ||
| ENST00000502751.5:n.329-15687G>A | ||
| NM_001282625.1:c.12G>A | NP_001269554.1:p.Pro4= | |
| NM_001282626.1:c.12G>A | NP_001269555.1:p.Pro4= | |
| NM_005572.3:c.12G>A , LRG_254t1:c.12G>A | NP_005563.1:p.Pro4= | |
| NM_170707.3:c.12G>A | NP_733821.1:p.Pro4= | |
| NM_170708.3:c.12G>A | NP_733822.1:p.Pro4= | |
| XR_921781.1:n.261G>A | ||
| XR_921781.2:n.259G>A | ||
| NM_170707.4:c.12G>A MANE Select | NP_733821.1:p.Pro4= | |
| NM_001282626.2:c.12G>A | NP_001269555.1:p.Pro4= | |
| NM_001282625.2:c.12G>A | NP_001269554.1:p.Pro4= | |
| NM_005572.4:c.12G>A MANE Plus Clinical | NP_005563.1:p.Pro4= | |
| NM_170708.4:c.12G>A | NP_733822.1:p.Pro4= |