Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232670A= , CM000667.2:g.173232670A= | GRCh38 |
| NC_000005.9:g.172659673A= , CM000667.1:g.172659673A= | GRCh37 |
| NC_000005.8:g.172592279A= | NCBI36 |
| NG_013340.1:g.7643T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329198.5:c.874T= MANE Select | ENSP00000327758.4:p.Phe292= | |
| ENST00000329198.4:c.874T= | ENSP00000327758.4:p.Phe292= | |
| NM_001166175.1:c.*827T= | NP_001159647.1:n.*827T= | |
| NM_001166176.1:c.*673T= | NP_001159648.1:n.*673T= | |
| NM_004387.3:c.874T= | NP_004378.1:p.Phe292= | |
| NM_004387.4:c.874T= MANE Select | NP_004378.1:p.Phe292= | |
| NM_001166175.2:c.*827T= | NP_001159647.1:n.*827T= | |
| NM_001166176.2:c.*673T= | NP_001159648.1:n.*673T= |