Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29588982C>G , CM000668.2:g.29588982C>G | GRCh38 |
| NC_000006.11:g.29556759C>G , CM000668.1:g.29556759C>G | GRCh37 |
| NC_000006.10:g.29664738C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641840.1:c.*99C>G (OR2H2) MANE Select | ENSP00000492959.1:n.*99C>G | |
| ENST00000355973.7:c.*2+14559G>C (GABBR1) | ENSP00000348248.3:n.*2+14559G>C | |
| ENST00000383640.3:c.*99C>G (OR2H2) | ENSP00000373136.2:n.*99C>G | |
| XM_011514911.1:c.*99C>G (OR2H2) | XP_011513213.1:n.*99C>G | |
| XM_011514912.1:c.882+156C>G (OR2H2) | XP_011513214.1:n.882+156C>G | |
| XM_011514912.3:c.882+156C>G (OR2H2) | XP_011513214.1:n.882+156C>G | |
| NM_007160.4:c.*99C>G (OR2H2) MANE Select | NP_009091.3:n.*99C>G |