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