Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.121941817A= , CM000665.2:g.121941817A= | GRCh38 |
| NC_000003.11:g.121660664A= , CM000665.1:g.121660664A= | GRCh37 |
| NC_000003.10:g.123143354A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021082.4:c.*810A= MANE Select | NP_066568.3:n.*810A= |
| ENST00000489711.6:c.*810A= MANE Select | ENSP00000417085.1:n.*810A= |
| NM_001145998.1:c.*810A= | NP_001139470.1:n.*810A= |
| NM_001145998.2:c.*810A= | NP_001139470.1:n.*810A= |
| NM_021082.3:c.*810A= | NP_066568.3:n.*810A= |
| ENST00000489711.5:c.*810A= | ENSP00000417085.1:n.*810A= |
| XM_005247722.2:c.*810A= | XP_005247779.1:n.*810A= |
| XM_005247722.3:c.*810A= | XP_005247779.1:n.*810A= |