Linked Data
dbSNP Id:
rs1813579606
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127079912A>G , CM000670.2:g.127079912A>G | GRCh38 |
| NC_000008.10:g.128092157A>G , CM000670.1:g.128092157A>G | GRCh37 |
| NC_000008.9:g.128161339A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109833.1:n.39A>G (PRNCR1) | ||
| NR_119373.1:n.102-779T>C (PCAT2) |