Linked Data
ClinVar Variation Id:
46884
ClinVar RCV Id:
RCV000040154
RCV000250652
RCV000845348
RCV001083883
RCV001130222
RCV001130223
RCV000770060
RCV001130922
RCV001130923
RCV001130924
dbSNP Id:
rs115744476
ExAC:
2:179547455 T / C
gnomAD v2:
2-179547455-T-C
gnomAD v3:
2-178682728-T-C
gnomAD v4:
2-178682728-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178682728T>C , CM000664.2:g.178682728T>C | GRCh38 |
| NC_000002.11:g.179547455T>C , CM000664.1:g.179547455T>C | GRCh37 |
| NC_000002.10:g.179255700T>C | NCBI36 |
| NG_011618.3:g.153075A>G , LRG_391:g.153075A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.29331A>G | ENSP00000343764.6:p.Glu9777= | |
| ENST00000342175.11:c.13859-40411A>G | ENSP00000340554.6:n.13859-40411A>G | |
| ENST00000359218.10:c.13658-40411A>G | ENSP00000352154.5:n.13658-40411A>G | |
| ENST00000342175.10:c.13859-40411A>G | ENSP00000340554.6:n.13859-40411A>G | |
| ENST00000342992.10:c.29331A>G | ENSP00000343764.6:p.Glu9777= | |
| ENST00000359218.9:c.13658-40411A>G | ENSP00000352154.5:n.13658-40411A>G | |
| ENST00000414766.5:c.1905A>G | ENSP00000401501.1:p.Glu635= | |
| ENST00000460472.6:c.13283-40411A>G | ENSP00000434586.1:n.13283-40411A>G | |
| ENST00000589042.5:c.33063A>G MANE Select | ENSP00000467141.1:p.Glu11021= | |
| ENST00000591111.5:c.32112A>G | ENSP00000465570.1:p.Glu10704= | |
| ENST00000615779.4:c.32112A>G | ENSP00000483597.1:p.Glu10704= | |
| NM_001256850.1:c.32112A>G | NP_001243779.1:p.Glu10704= | |
| NM_001267550.2:c.33063A>G MANE Select | NP_001254479.2:p.Glu11021= | |
| NM_003319.4:c.13283-40411A>G | NP_003310.4:n.13283-40411A>G | |
| NM_133378.4:c.29331A>G | NP_596869.4:p.Glu9777= | |
| NM_133432.3:c.13658-40411A>G | NP_597676.3:n.13658-40411A>G | |
| NM_133437.4:c.13859-40411A>G | NP_597681.4:n.13859-40411A>G | |
| XM_011511729.1:c.32160A>G | XP_011510031.1:p.Glu10720= | |
| XM_011511730.1:c.13469-40411A>G | XP_011510032.1:n.13469-40411A>G | |
| XM_011511731.1:c.13328-40411A>G | XP_011510033.1:n.13328-40411A>G | |
| XM_017004819.1:c.32115A>G | XP_016860308.1:p.Glu10705= | |
| XM_017004820.1:c.29334A>G | XP_016860309.1:p.Glu9778= | |
| XM_017004821.1:c.29331A>G | XP_016860310.1:p.Glu9777= | |
| XM_017004822.1:c.31323A>G | XP_016860311.1:p.Glu10441= | |
| XM_017004823.1:c.13424-40411A>G | XP_016860312.1:n.13424-40411A>G | |
| XM_024453094.1:c.32115A>G | XP_024308862.1:p.Glu10705= | |
| XM_024453095.1:c.32115A>G | XP_024308863.1:p.Glu10705= | |
| XM_024453096.1:c.32115A>G | XP_024308864.1:p.Glu10705= | |
| XM_024453097.1:c.31155A>G | XP_024308865.1:p.Glu10385= | |
| XM_024453098.1:c.31074A>G | XP_024308866.1:p.Glu10358= | |
| XM_024453099.1:c.13424-40411A>G | XP_024308867.1:n.13424-40411A>G |