Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88719719A= , CM000678.2:g.88719719A= | GRCh38 |
| NC_000016.9:g.88786127A= , CM000678.1:g.88786127A= | GRCh37 |
| NC_000016.8:g.87313628A= | NCBI36 |
| NG_042229.1:g.70502T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.6326T= MANE Select | ENSP00000301015.9:p.Phe2109= | |
| ENST00000466823.3:c.352T= | ||
| ENST00000301015.13:c.6326T= | ENSP00000301015.9:p.Phe2109= | |
| ENST00000419505.5:c.92T= | ENSP00000406358.1:p.Phe31= | |
| ENST00000466823.2:c.352T= | ||
| ENST00000495568.7:n.567T= | ||
| ENST00000497793.2:n.481T= | ||
| NM_001142864.2:c.6326T= | NP_001136336.2:p.Phe2109= | |
| NM_001142864.3:c.6326T= | NP_001136336.2:p.Phe2109= | |
| NM_001142864.4:c.6326T= MANE Select | NP_001136336.2:p.Phe2109= |