Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48417317T= , CM000674.2:g.48417317T= | GRCh38 |
| NC_000012.11:g.48811100T= , CM000674.1:g.48811100T= | GRCh37 |
| NC_000012.10:g.47097367T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| ENST00000609970.1:n.21A= (OR8S21P) | |
| XM_011537896.2:c.-449+3735T= (C12orf54) | XP_011536198.1:n.-449+3735T= |
| XM_017018796.1:c.-523+3735T= (C12orf54) | XP_016874285.1:n.-523+3735T= |