Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.122661792C>T , CM000671.2:g.122661792C>T | GRCh38 |
| NC_000009.11:g.125424071C>T , CM000671.1:g.125424071C>T | GRCh37 |
| NC_000009.10:g.124463892C>T | NCBI36 |
| NG_034002.1:g.5077C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001005236.3:c.77C>T (OR1L1) MANE Select | NP_001005236.3:p.Pro26Leu |
| ENST00000309623.1:c.77C>T (OR1L1) MANE Select | ENSP00000310773.1:p.Pro26Leu |
| ENST00000373686.1:c.227C>T (OR1L1) | ENSP00000362790.1:p.Pro76Leu |
| XM_011518243.1:c.-685-4167G>A (OR1L8) | XP_011516545.1:n.-685-4167G>A |