Linked Data
dbSNP Id:
rs1579879342
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.61203278C>T , CM000667.2:g.61203278C>T | GRCh38 |
| NC_000005.9:g.60499105C>T , CM000667.1:g.60499105C>T | GRCh37 |
| NC_000005.8:g.60534862C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109908.1:n.422+22840C>T (SMIM15-AS1) | ||
| XR_948364.1:n.731-1574G>A (LINC02057) |