Linked Data
ClinVar Variation Id:
1083722
dbSNP Id:
rs2144406775
MyVariant Identifiers:
chr18:g.29172945G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31592982G>A , CM000680.2:g.31592982G>A | GRCh38 |
| NC_000018.9:g.29172945G>A , CM000680.1:g.29172945G>A | GRCh37 |
| NC_000018.8:g.27426943G>A | NCBI36 |
| NG_009490.1:g.6216G>A , LRG_416:g.6216G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.156G>A MANE Select | ENSP00000237014.4:p.Val52= | |
| ENST00000610404.5:c.60G>A | ENSP00000477599.2:p.Val20= | |
| ENST00000649620.1:c.156G>A | ENSP00000497927.1:p.Val52= | |
| ENST00000237014.7:c.156G>A | ENSP00000237014.3:p.Val52= | |
| ENST00000432547.7:n.182G>A | ||
| ENST00000541025.2:n.182G>A | ||
| ENST00000610404.4:c.156G>A | ENSP00000477599.1:p.Val52= | |
| ENST00000613781.1:c.156G>A | ENSP00000479174.1:p.Val52= | |
| NM_000371.3:c.156G>A , LRG_416t1:c.156G>A | NP_000362.1:p.Val52= | |
| NM_000371.4:c.156G>A MANE Select | NP_000362.1:p.Val52= |