dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.110091706A>C , CM000673.2:g.110091706A>C | GRCh38 |
| NC_000011.9:g.109962432A>C , CM000673.1:g.109962432A>C | GRCh37 |
| NC_000011.8:g.109467642A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645527.1:c.*757+32353T>G (RDX) | ENSP00000496121.1:n.*757+32353T>G | |
| XM_011543056.1:c.-73+3105A>C (ZC3H12C) | XP_011541358.1:n.-73+3105A>C |