Linked Data
dbSNP Id:
rs960689826
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.61203439T>G , CM000667.2:g.61203439T>G | GRCh38 |
| NC_000005.9:g.60499266T>G , CM000667.1:g.60499266T>G | GRCh37 |
| NC_000005.8:g.60535023T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109908.1:n.422+23001T>G (SMIM15-AS1) | ||
| XR_948364.1:n.731-1735A>C (LINC02057) |