Linked Data
dbSNP Id:
rs1005747902
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.51845078C>G , CM000664.2:g.51845078C>G | GRCh38 |
| NC_000002.11:g.52072216C>G , CM000664.1:g.52072216C>G | GRCh37 |
| NC_000002.10:g.51925720C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245003.1:n.840-16371C>G | ||
| NR_135237.1:n.840-16371C>G |