Linked Data
dbSNP Id:
rs2070421098
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49363131G>A , CM000679.2:g.49363131G>A | GRCh38 |
| NC_000017.10:g.47440493G>A , CM000679.1:g.47440493G>A | GRCh37 |
| NC_000017.9:g.44795492G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110882.1:n.136+614G>A | ||
| NR_110883.1:n.31-1148G>A | ||
| NR_110884.1:n.58-1148G>A |