gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.91351335G>C , CM000675.2:g.91351335G>C | GRCh38 |
| NC_000013.10:g.92003589G>C , CM000675.1:g.92003589G>C | GRCh37 |
| NC_000013.9:g.90801590G>C | NCBI36 |
| NG_032702.1:g.8516G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027349.1:n.284+1109G>C (MIR17HG) | ||
| NR_027350.1:n.1778G>C (MIR17HG) | ||
| NR_029508.1:n.22G>C (MIR92A1) |