Linked Data
ClinVar Variation Id:
1002952
ClinVar RCV Id:
RCV001299447
dbSNP Id:
rs2038702963
gnomAD v4:
19-50402692-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.50402692T>G , CM000681.2:g.50402692T>G | GRCh38 |
| NC_000019.9:g.50905949T>G , CM000681.1:g.50905949T>G | GRCh37 |
| NC_000019.8:g.55597761T>G | NCBI36 |
| NG_033800.1:g.23370T>G , LRG_785:g.23370T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593887.2:c.921T>G | ENSP00000472607.2:p.Ile307Met | |
| ENST00000600746.2:n.1112T>G | ||
| ENST00000644560.2:c.921T>G | ENSP00000495618.2:p.Ile307Met | |
| ENST00000687454.1:c.921T>G | ENSP00000510052.1:p.Ile307Met | |
| ENST00000440232.7:c.921T>G MANE Select | ENSP00000406046.1:p.Ile307Met | |
| ENST00000595904.6:c.921T>G | ENSP00000472445.1:p.Ile307Met | |
| ENST00000599857.7:c.921T>G | ENSP00000473052.1:p.Ile307Met | |
| ENST00000601098.6:c.921T>G | ENSP00000472600.2:p.Ile307Met | |
| ENST00000613923.6:c.921T>G | ENSP00000481858.2:p.Ile307Met | |
| ENST00000643407.1:c.921T>G | ENSP00000496078.1:p.Ile307Met | |
| ENST00000440232.6:c.921T>G | ENSP00000406046.1:p.Ile307Met | |
| ENST00000595904.5:c.921T>G | ENSP00000472445.1:p.Ile307Met | |
| ENST00000599857.5:c.921T>G | ENSP00000473052.1:p.Ile307Met | |
| ENST00000600859.5:c.921T>G | ENSP00000470726.1:p.Ile307Met | |
| ENST00000613923.4:c.921T>G | ENSP00000481858.1:p.Ile307Met | |
| NM_001256849.1:c.921T>G , LRG_785t1:c.921T>G | NP_001243778.1:p.Ile307Met | |
| NM_001308632.1:c.921T>G , LRG_785t2:c.921T>G | NP_001295561.1:p.Ile307Met | |
| NM_002691.3:c.921T>G | NP_002682.2:p.Ile307Met | |
| NR_046402.1:n.990T>G | ||
| XM_005259008.3:c.921T>G | XP_005259065.1:p.Ile307Met | |
| XM_011527038.1:c.921T>G | XP_011525340.1:p.Ile307Met | |
| XM_011527039.1:c.921T>G | XP_011525341.1:p.Ile307Met | |
| XR_935835.1:n.1023T>G | ||
| XM_005259008.4:c.921T>G | XP_005259065.1:p.Ile307Met | |
| XM_017026881.1:c.921T>G | XP_016882370.1:p.Ile307Met | |
| XM_017026882.2:c.921T>G | XP_016882371.1:p.Ile307Met | |
| XR_935835.2:n.1022T>G | ||
| NM_002691.4:c.921T>G MANE Select | NP_002682.2:p.Ile307Met | |
| NR_046402.2:n.966T>G |