Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97395908C>T , CM000677.2:g.97395908C>T | GRCh38 |
| NC_000015.9:g.97939138C>T , CM000677.1:g.97939138C>T | GRCh37 |
| NC_000015.8:g.95740142C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120324.1:n.755+1749G>A (LINC02254) | ||
| XR_001751693.1:n.305-15284C>T (LINC02253) | ||
| XR_001751694.1:n.305-15284C>T (LINC02253) | ||
| XR_001751695.1:n.305-15284C>T (LINC02253) |