Linked Data
dbSNP Id:
rs2134667509
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.130403388A>G , CM000673.2:g.130403388A>G | GRCh38 |
| NC_000011.9:g.130273283A>G , CM000673.1:g.130273283A>G | GRCh37 |
| NC_000011.8:g.129778493A>G | NCBI36 |
| NG_052870.1:g.30606T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948177.1:n.2483A>G | ||
| XR_948178.1:n.2137A>G | ||
| XR_948179.1:n.2055A>G | ||
| XR_948180.1:n.2055A>G | ||
| XR_948181.1:n.624A>G | ||
| XR_948182.1:n.2215A>G | ||
| XR_948183.1:n.458+9589A>G | ||
| XR_948184.1:n.546A>G | ||
| XR_948185.1:n.475A>G | ||
| XR_948187.1:n.458+9589A>G | ||
| XR_948188.1:n.378A>G | ||
| XR_948189.1:n.426A>G | ||
| NR_148980.1:n.699A>G |