Linked Data
dbSNP Id:
rs2066217699
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658216T>A , CM000684.2:g.21658216T>A | GRCh38 |
| NC_000022.10:g.22012505T>A , CM000684.1:g.22012505T>A | GRCh37 |
| NC_000022.9:g.20342505T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.163-50T>A | ||
| ENST00000498589.1:n.343-50T>A | ||
| XM_017029165.1:c.478-50T>A | XP_016884654.1:n.478-50T>A | |
| NR_169729.1:n.1028T>A | ||
| NR_169730.1:n.931T>A | ||
| NR_169731.1:n.432-2621T>A | ||
| NR_169732.1:n.132-50T>A | ||
| NR_169733.1:n.214-74T>A | ||
| NR_169734.1:n.214-50T>A |