Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.73321002A>G , CM000670.2:g.73321002A>G | GRCh38 |
| NC_000008.10:g.74233237A>G , CM000670.1:g.74233237A>G | GRCh37 |
| NC_000008.9:g.74395791A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000240285.10:c.695A>G (RDH10) MANE Select | ENSP00000240285.5:p.Glu232Gly | |
| ENST00000240285.9:c.695A>G (RDH10) | ENSP00000240285.5:p.Glu232Gly | |
| ENST00000519380.1:c.200A>G (RDH10) | ENSP00000428132.1:p.Glu67Gly | |
| NM_172037.4:c.695A>G (RDH10) | NP_742034.1:p.Glu232Gly | |
| NR_125388.1:n.729+738T>C (RDH10-AS1) | ||
| XM_011517466.1:c.200A>G (RDH10) | XP_011515768.1:p.Glu67Gly | |
| NM_172037.5:c.695A>G (RDH10) MANE Select | NP_742034.1:p.Glu232Gly |