Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.158755516T>C , CM000663.2:g.158755516T>C | GRCh38 |
| NC_000001.10:g.158725306T>C , CM000663.1:g.158725306T>C | GRCh37 |
| NC_000001.9:g.156991930T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001005184.2:c.629T>C (OR6K6) MANE Select | NP_001005184.2:p.Ile210Thr |
| ENST00000641861.1:c.629T>C (OR6K6) MANE Select | ENSP00000493180.1:p.Ile210Thr |
| NM_001005184.1:c.701T>C (OR6K6) | NP_001005184.1:p.Ile234Thr |
| ENST00000368144.2:c.701T>C (OR6K6) | ENSP00000357126.2:p.Ile234Thr |
| ENST00000641189.1:n.176-7617A>G (OR6N1) | |
| XR_001736980.1:n.841-7617A>G (OR6N1) |