Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165069129A= , CM000665.2:g.165069129A= | GRCh38 |
| NC_000003.11:g.164786917A= , CM000665.1:g.164786917A= | GRCh37 |
| NC_000003.10:g.166269611A= | NCBI36 |
| NG_017043.1:g.14367T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264382.8:c.322T= MANE Select | ENSP00000264382.3:p.Phe108= | |
| ENST00000264382.7:c.322T= | ENSP00000264382.3:p.Phe108= | |
| ENST00000476593.1:c.*197T= | ENSP00000419450.1:n.*197T= | |
| NM_001041.3:c.322T= | NP_001032.2:p.Phe108= | |
| XM_011513078.1:c.223T= | XP_011511380.1:p.Phe75= | |
| XM_011513078.2:c.223T= | XP_011511380.1:p.Phe75= | |
| NM_001041.4:c.322T= MANE Select | NP_001032.2:p.Phe108= |