Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.68836777G>C , CM000664.2:g.68836777G>C | GRCh38 |
| NC_000002.11:g.69063909G>C , CM000664.1:g.69063909G>C | GRCh37 |
| NC_000002.10:g.68917413G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001739529.2:n.612C>G (LINC01890) | |
| XR_001739530.1:n.862-605G>C (LINC01888) | |
| XR_940226.1:n.431C>G (LINC01890) | |
| XR_940226.3:n.612C>G (LINC01890) |