Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.101806214C>G , CM000677.2:g.101806214C>G | GRCh38 |
| NC_000015.9:g.102346417C>G , CM000677.1:g.102346417C>G | GRCh37 |
| NC_000015.8:g.100163940C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001005326.2:c.495C>G (OR4F6) MANE Select | NP_001005326.1:p.Asp165Glu |
| ENST00000328882.6:c.495C>G (OR4F6) MANE Select | ENSP00000327525.4:p.Asp165Glu |
| NM_001005326.1:c.495C>G (OR4F6) | NP_001005326.1:p.Asp165Glu |
| ENST00000328882.5:c.495C>G (OR4F6) | ENSP00000327525.4:p.Asp165Glu |
| ENST00000536946.2:c.407+88C>G (OR4F15) | ENSP00000481880.1:n.407+88C>G |