Linked Data
dbSNP Id:
rs2095145765
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.5857228T>G , CM000680.2:g.5857228T>G | GRCh38 |
| NC_000018.9:g.5857227T>G , CM000680.1:g.5857227T>G | GRCh37 |
| NC_000018.8:g.5847227T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_172494.1:n.603-21215T>G | ||
| NR_172495.1:n.603-19025T>G | ||
| NR_172496.1:n.603-19025T>G | ||
| NR_172497.1:n.603-19025T>G | ||
| NR_172498.1:n.663-9885T>G | ||
| NR_172499.1:n.603-19025T>G | ||
| NR_172500.1:n.603-19025T>G | ||
| NR_172501.1:n.603-19025T>G | ||
| NR_172502.1:n.603-19025T>G | ||
| NR_172503.1:n.603-19025T>G |