dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.128008933G>C , CM000670.2:g.128008933G>C | GRCh38 |
| NC_000008.10:g.129021179G>C , CM000670.1:g.129021179G>C | GRCh37 |
| NC_000008.9:g.129090361G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003367.3:n.1212+19642G>C (PVT1) | ||
| NR_031611.1:n.36G>C (MIR1206) |