| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.94834510G= , CM000674.2:g.94834510G= | GRCh38 |
| NC_000012.11:g.95228286G= , CM000674.1:g.95228286G= | GRCh37 |
| NC_000012.10:g.93752417G= | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| NR_030171.1:n.113G= (MIR492) | |
| NR_036685.1:n.57G= (KRT19P2) | |
| ENST00000405395.2:n.57G= (KRT19P2) | |
| ENST00000557173.1:n.364G= (KRT19P2) |