Linked Data
dbSNP Id:
rs2070423998
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.49363382C>T , CM000679.2:g.49363382C>T | GRCh38 |
| NC_000017.10:g.47440744C>T , CM000679.1:g.47440744C>T | GRCh37 |
| NC_000017.9:g.44795743C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110882.1:n.136+865C>T | ||
| NR_110883.1:n.31-897C>T | ||
| NR_110884.1:n.58-897C>T |