Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.51186580G= , CM000677.2:g.51186580G= | GRCh38 |
| NC_000015.9:g.51478777G= , CM000677.1:g.51478777G= | GRCh37 |
| NC_000015.8:g.49266069G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_146310.1:n.195-91403G= (MIR4713HG) | |
| XR_932222.1:n.99-91403G= (PIRC66) |