Linked Data
dbSNP Id:
rs1688513056
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203856880A>G , CM000664.2:g.203856880A>G | GRCh38 |
| NC_000002.11:g.204721603A>G , CM000664.1:g.204721603A>G | GRCh37 |
| NC_000002.10:g.204429848A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696479.1:c.47+2804A>G | ENSP00000512655.1:n.47+2804A>G | |
| XR_923797.1:n.225-5593A>G |