Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.97396032T>C , CM000677.2:g.97396032T>C | GRCh38 |
| NC_000015.9:g.97939262T>C , CM000677.1:g.97939262T>C | GRCh37 |
| NC_000015.8:g.95740266T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_120324.1:n.755+1625A>G (LINC02254) | ||
| XR_001751693.1:n.305-15160T>C (LINC02253) | ||
| XR_001751694.1:n.305-15160T>C (LINC02253) | ||
| XR_001751695.1:n.305-15160T>C (LINC02253) |