Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.56050233C>T , CM000680.2:g.56050233C>T | GRCh38 |
| NC_000018.9:g.53717464C>T , CM000680.1:g.53717464C>T | GRCh37 |
| NC_000018.8:g.51868462C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_146510.1:n.165+56C>T (LINC01905) | |
| NR_146511.1:n.165+56C>T (LINC01905) | |
| NR_148972.1:n.1067+5672G>A (LINC03069) |