Linked Data
dbSNP Id:
rs1879685060
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.84458241T>C , CM000675.2:g.84458241T>C | GRCh38 |
| NC_000013.10:g.85032376T>C , CM000675.1:g.85032376T>C | GRCh37 |
| NC_000013.9:g.83930377T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_046871.1:n.139-104123T>C | ||
| XR_942133.1:n.369-46322A>G | ||
| XR_942134.1:n.366-46322A>G |