Linked Data
ClinVar Variation Id:
1984076
ClinVar RCV Id:
RCV002775319
dbSNP Id:
rs770174208
ExAC:
11:71146809 C / A
gnomAD v2:
11-71146809-C-A
gnomAD v3:
11-71435763-C-A
gnomAD v4:
11-71435763-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.71435763C>A , CM000673.2:g.71435763C>A | GRCh38 |
| NC_000011.9:g.71146809C>A , CM000673.1:g.71146809C>A | GRCh37 |
| NC_000011.8:g.70824457C>A | NCBI36 |
| NG_012655.2:g.17669G>T , LRG_340:g.17669G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525346.6:c.1040G>T | ENSP00000435707.3:p.Gly347Val | |
| ENST00000526780.6:c.1040G>T | ENSP00000435668.2:p.Gly347Val | |
| ENST00000527316.6:c.866G>T | ENSP00000435047.2:p.Gly289Val | |
| ENST00000682708.1:c.1091G>T | ENSP00000506866.1:p.Gly364Val | |
| ENST00000683287.1:c.1076G>T | ENSP00000507607.1:p.Gly359Val | |
| ENST00000683714.1:c.1048G>T | ENSP00000508207.1:p.Ala350Ser | |
| ENST00000684396.1:n.1080G>T | ||
| ENST00000685320.1:c.455G>T | ENSP00000509319.1:p.Gly152Val | |
| ENST00000690257.1:c.944G>T | ENSP00000510750.1:p.Gly315Val | |
| ENST00000355527.8:c.1040G>T MANE Select | ENSP00000347717.4:p.Gly347Val | |
| ENST00000355527.7:c.1040G>T | ENSP00000347717.3:p.Gly347Val | |
| ENST00000407721.6:c.1040G>T | ENSP00000384739.2:p.Gly347Val | |
| ENST00000525137.1:c.541G>T | ENSP00000435956.1:p.Ala181Ser | |
| ENST00000533800.5:c.290G>T | ENSP00000435011.1:p.Gly97Val | |
| ENST00000534795.5:c.319+2049G>T | ||
| NM_001163817.1:c.1040G>T | NP_001157289.1:p.Gly347Val | |
| NM_001360.2:c.1040G>T , LRG_340t1:c.1040G>T | NP_001351.2:p.Gly347Val | |
| XM_011544777.1:c.1174G>T | XP_011543079.1:p.Ala392Ser | |
| XM_011544777.2:c.1174G>T | XP_011543079.1:p.Ala392Ser | |
| NM_001163817.2:c.1040G>T | NP_001157289.1:p.Gly347Val | |
| NM_001360.3:c.1040G>T MANE Select | NP_001351.2:p.Gly347Val |