Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312774T>A , CM000673.2:g.118312774T>A | GRCh38 |
| NC_000011.9:g.118183489T>A , CM000673.1:g.118183489T>A | GRCh37 |
| NC_000011.8:g.117688699T>A | NCBI36 |
| NG_007383.1:g.13195T>A , LRG_38:g.13195T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.260T>A MANE Select | ENSP00000354566.4:p.Phe87Tyr | |
| ENST00000361763.8:c.260T>A | ENSP00000354566.4:p.Phe87Tyr | |
| ENST00000526146.5:n.806T>A | ||
| ENST00000528435.5:n.813T>A | ||
| ENST00000528600.1:c.242T>A | ENSP00000433975.1:p.Phe81Tyr | |
| ENST00000529713.5:n.366T>A | ||
| ENST00000531913.1:n.631T>A | ||
| NM_000733.3:c.260T>A , LRG_38t1:c.260T>A | NP_000724.1:p.Phe87Tyr | |
| NM_000733.4:c.260T>A MANE Select | NP_000724.1:p.Phe87Tyr |