Linked Data
dbSNP Id:
rs2051786342
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.64209862T>C , CM000680.2:g.64209862T>C | GRCh38 |
| NC_000018.9:g.61877097T>C , CM000680.1:g.61877097T>C | GRCh37 |
| NC_000018.8:g.60028077T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_033881.1:n.201-39439T>C |