Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965403A>T , CM000670.2:g.37965403A>T | GRCh38 |
| NC_000008.10:g.37822921A>T , CM000670.1:g.37822921A>T | GRCh37 |
| NC_000008.9:g.37942078A>T | NCBI36 |
| NG_011936.1:g.6264T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000025.3:c.1067T>A MANE Select | NP_000016.1:p.Phe356Tyr |
| ENST00000345060.5:c.1067T>A MANE Select | ENSP00000343782.3:p.Phe356Tyr |
| NM_000025.2:c.1067T>A | NP_000016.1:p.Phe356Tyr |
| ENST00000345060.4:c.1067T>A | ENSP00000343782.3:p.Phe356Tyr |
| ENST00000520341.1:n.342T>A | |
| ENST00000520341.2:n.1195T>A | |
| ENST00000614635.1:c.1067T>A | ENSP00000480325.1:p.Phe356Tyr |
| ENST00000647937.1:c.551T>A | ENSP00000497740.1:p.Phe184Tyr |