Linked Data
dbSNP Id:
rs1020869882
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.51935839G>T , CM000664.2:g.51935839G>T | GRCh38 |
| NC_000002.11:g.52162977G>T , CM000664.1:g.52162977G>T | GRCh37 |
| NC_000002.10:g.52016481G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245003.1:n.879+74351G>T | ||
| NR_135237.1:n.879+74351G>T |