Linked Data
dbSNP Id:
rs2138025845
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303687G>C , CM000675.2:g.48303687G>C | GRCh38 |
| NC_000013.10:g.48877823G>C , CM000675.1:g.48877823G>C | GRCh37 |
| NC_000013.9:g.47775824G>C | NCBI36 |
| NG_009009.1:g.4941G>C , LRG_517:g.4941G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046414.2:n.16C>G |