Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.21340975A>G , CM000675.2:g.21340975A>G | GRCh38 |
| NC_000013.10:g.21915114A>G , CM000675.1:g.21915114A>G | GRCh37 |
| NC_000013.9:g.20813114A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_046461.1:n.439-10173A>G (MIPEPP3) | ||
| NR_103840.1:n.121+3691T>C (LINC00539) | ||
| NR_103841.1:n.194+3691T>C (LINC00539) |