Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965787A>T , CM000670.2:g.37965787A>T | GRCh38 |
| NC_000008.10:g.37823305A>T , CM000670.1:g.37823305A>T | GRCh37 |
| NC_000008.9:g.37942462A>T | NCBI36 |
| NG_011936.1:g.5880T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.683T>A MANE Select | NP_000016.1:p.Phe228Tyr |
| ENST00000345060.5:c.683T>A MANE Select | ENSP00000343782.3:p.Phe228Tyr |
| NM_000025.2:c.683T>A | NP_000016.1:p.Phe228Tyr |
| ENST00000345060.4:c.683T>A | ENSP00000343782.3:p.Phe228Tyr |
| ENST00000520341.2:n.811T>A | |
| ENST00000614635.1:c.683T>A | ENSP00000480325.1:p.Phe228Tyr |
| ENST00000647937.1:c.167T>A | ENSP00000497740.1:p.Phe56Tyr |