Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49950856T= , CM000674.2:g.49950856T= | GRCh38 |
| NC_000012.11:g.50344639T= , CM000674.1:g.50344639T= | GRCh37 |
| NC_000012.10:g.48630906T= | NCBI36 |
| NG_008913.1:g.5116T= , LRG_717:g.5116T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000199280.4:c.26T= MANE Select | ENSP00000199280.3:p.Phe9= | |
| ENST00000199280.3:c.26T= | ENSP00000199280.3:p.Phe9= | |
| ENST00000550862.1:c.26T= | ENSP00000450022.1:p.Phe9= | |
| ENST00000551526.5:c.26T= | ENSP00000447148.1:p.Phe9= | |
| NM_000486.5:c.26T= , LRG_717t1:c.26T= | NP_000477.1:p.Phe9= | |
| NM_000486.6:c.26T= MANE Select | NP_000477.1:p.Phe9= |