Linked Data
ClinVar Variation Id:
2785768
ClinVar RCV Id:
RCV003627004
dbSNP Id:
rs1231398400
gnomAD v2:
18-29175215-A-G
gnomAD v4:
18-31595252-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31595252A>G , CM000680.2:g.31595252A>G | GRCh38 |
| NC_000018.9:g.29175215A>G , CM000680.1:g.29175215A>G | GRCh37 |
| NC_000018.8:g.27429213A>G | NCBI36 |
| NG_009490.1:g.8486A>G , LRG_416:g.8486A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.333A>G MANE Select | ENSP00000237014.4:p.Ala111= | |
| ENST00000610404.5:c.237A>G | ENSP00000477599.2:p.Ala79= | |
| ENST00000649620.1:c.333A>G | ENSP00000497927.1:p.Ala111= | |
| ENST00000237014.7:c.333A>G | ENSP00000237014.3:p.Ala111= | |
| ENST00000541025.2:n.359A>G | ||
| ENST00000610404.4:c.333A>G | ENSP00000477599.1:p.Ala111= | |
| ENST00000613781.1:c.333A>G | ENSP00000479174.1:p.Ala111= | |
| NM_000371.3:c.333A>G , LRG_416t1:c.333A>G | NP_000362.1:p.Ala111= | |
| NM_000371.4:c.333A>G MANE Select | NP_000362.1:p.Ala111= |