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