Linked Data
ClinVar Variation Id:
229427
ClinVar RCV Id:
RCV000217136
RCV000726852
RCV001129316
RCV001129315
RCV001129317
RCV001129318
RCV001129319
dbSNP Id:
rs774557269
ExAC:
2:179516471 C / T
gnomAD v2:
2-179516471-C-T
gnomAD v3:
2-178651744-C-T
gnomAD v4:
2-178651744-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178651744C>T , CM000664.2:g.178651744C>T | GRCh38 |
| NC_000002.11:g.179516471C>T , CM000664.1:g.179516471C>T | GRCh37 |
| NC_000002.10:g.179224716C>T | NCBI36 |
| NG_011618.3:g.184059G>A , LRG_391:g.184059G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342992.11:c.32083G>A | ENSP00000343764.6:p.Val10695Ile | |
| ENST00000342175.11:c.13859-9427G>A | ENSP00000340554.6:n.13859-9427G>A | |
| ENST00000359218.10:c.13658-9427G>A | ENSP00000352154.5:n.13658-9427G>A | |
| ENST00000342175.10:c.13859-9427G>A | ENSP00000340554.6:n.13859-9427G>A | |
| ENST00000342992.10:c.32083G>A | ENSP00000343764.6:p.Val10695Ile | |
| ENST00000359218.9:c.13658-9427G>A | ENSP00000352154.5:n.13658-9427G>A | |
| ENST00000414766.5:c.2441-9427G>A | ENSP00000401501.1:n.2441-9427G>A | |
| ENST00000460472.6:c.13283-9427G>A | ENSP00000434586.1:n.13283-9427G>A | |
| ENST00000589042.5:c.39385G>A MANE Select | ENSP00000467141.1:p.Val13129Ile | |
| ENST00000591111.5:c.34864G>A | ENSP00000465570.1:p.Val11622Ile | |
| ENST00000615779.4:c.34864G>A | ENSP00000483597.1:p.Val11622Ile | |
| NM_001256850.1:c.34864G>A | NP_001243779.1:p.Val11622Ile | |
| NM_001267550.2:c.39385G>A MANE Select | NP_001254479.2:p.Val13129Ile | |
| NM_003319.4:c.13283-9427G>A | NP_003310.4:n.13283-9427G>A | |
| NM_133378.4:c.32083G>A | NP_596869.4:p.Val10695Ile | |
| NM_133432.3:c.13658-9427G>A | NP_597676.3:n.13658-9427G>A | |
| NM_133437.4:c.13859-9427G>A | NP_597681.4:n.13859-9427G>A | |
| XM_011511729.1:c.38482G>A | XP_011510031.1:p.Val12828Ile | |
| XM_011511730.1:c.13469-9427G>A | XP_011510032.1:n.13469-9427G>A | |
| XM_011511731.1:c.13328-9427G>A | XP_011510033.1:n.13328-9427G>A | |
| XM_017004819.1:c.38278G>A | XP_016860308.1:p.Val12760Ile | |
| XM_017004820.1:c.33676G>A | XP_016860309.1:p.Val11226Ile | |
| XM_017004821.1:c.33673G>A | XP_016860310.1:p.Val11225Ile | |
| XM_017004822.1:c.31859-9427G>A | XP_016860311.1:n.31859-9427G>A | |
| XM_017004823.1:c.13424-9427G>A | XP_016860312.1:n.13424-9427G>A | |
| XM_024453094.1:c.33826G>A | XP_024308862.1:p.Val11276Ile | |
| XM_024453095.1:c.33823G>A | XP_024308863.1:p.Val11275Ile | |
| XM_024453096.1:c.33256G>A | XP_024308864.1:p.Val11086Ile | |
| XM_024453097.1:c.31691-9427G>A | XP_024308865.1:n.31691-9427G>A | |
| XM_024453098.1:c.31610-9427G>A | XP_024308866.1:n.31610-9427G>A | |
| XM_024453099.1:c.13424-9427G>A | XP_024308867.1:n.13424-9427G>A | |
| XM_024453100.1:c.2134G>A | XP_024308868.1:p.Val712Ile |