Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33114463T>A , CM000665.2:g.33114463T>A | GRCh38 |
| NC_000003.11:g.33155955T>A , CM000665.1:g.33155955T>A | GRCh37 |
| NC_000003.10:g.33130959T>A | NCBI36 |
| NG_008122.1:g.5506T>A , LRG_4:g.5506T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320954.11:c.386T>A MANE Select | ENSP00000323696.5:p.Phe129Tyr | |
| ENST00000320954.10:c.386T>A | ENSP00000323696.5:p.Phe129Tyr | |
| ENST00000449224.1:c.386T>A | ENSP00000409997.1:p.Phe129Tyr | |
| NM_006371.4:c.386T>A , LRG_4t1:c.386T>A | NP_006362.1:p.Phe129Tyr | |
| NM_006371.5:c.386T>A MANE Select | NP_006362.1:p.Phe129Tyr | |
| NM_001393363.1:c.386T>A | NP_001380292.1:p.Phe129Tyr | |
| NM_001393364.1:c.386T>A | NP_001380293.1:p.Phe129Tyr | |
| NM_001393365.1:c.386T>A | NP_001380294.1:p.Phe129Tyr |