Linked Data
dbSNP Id:
rs2055059499
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.26866502G>C , CM000680.2:g.26866502G>C | GRCh38 |
| NC_000018.9:g.24446466G>C , CM000680.1:g.24446466G>C | GRCh37 |
| NC_000018.8:g.22700464G>C | NCBI36 |
| NG_029560.1:g.4251C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_026908.1:n.53+1142G>C |