Linked Data
dbSNP Id:
rs2121208899
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.105714973T>G , CM000674.2:g.105714973T>G | GRCh38 |
| NC_000012.11:g.106108751T>G , CM000674.1:g.106108751T>G | GRCh37 |
| NC_000012.10:g.104632881T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110108.1:n.54+10717T>G | ||
| NR_110109.1:n.55-189T>G | ||
| NR_110110.1:n.83+8117T>G | ||
| NR_110111.1:n.83+8117T>G | ||
| NR_110111.2:n.83+8117T>G |