Linked Data
dbSNP Id:
rs2089540731
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.85756993T>C , CM000677.2:g.85756993T>C | GRCh38 |
| NC_000015.9:g.86300224T>C , CM000677.1:g.86300224T>C | GRCh37 |
| NC_000015.8:g.84101228T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_120366.1:n.419+891A>G |