dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6871595A>C , CM000673.2:g.6871595A>C | GRCh38 |
| NC_000011.9:g.6892826A>C , CM000673.1:g.6892826A>C | GRCh37 |
| NC_000011.8:g.6849402A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641461.1:c.*929A>C (OR10A2) MANE Select | ENSP00000493131.1:n.*929A>C | |
| XM_011520058.1:c.-436+26498T>G (OR2AG2) | XP_011518360.1:n.-436+26498T>G | |
| XM_011520059.1:c.-436+26498T>G (OR2AG2) | XP_011518361.1:n.-436+26498T>G | |
| XM_011520060.1:c.-436+26498T>G (OR2AG2) | XP_011518362.1:n.-436+26498T>G | |
| XM_011520061.1:c.-436+52903T>G (OR2AG2) | XP_011518363.1:n.-436+52903T>G | |
| NM_001004460.2:c.*929A>C (OR10A2) MANE Select | NP_001004460.1:n.*929A>C |