Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33114462T>G , CM000665.2:g.33114462T>G | GRCh38 |
| NC_000003.11:g.33155954T>G , CM000665.1:g.33155954T>G | GRCh37 |
| NC_000003.10:g.33130958T>G | NCBI36 |
| NG_008122.1:g.5505T>G , LRG_4:g.5505T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000320954.11:c.385T>G MANE Select | ENSP00000323696.5:p.Phe129Val | |
| ENST00000320954.10:c.385T>G | ENSP00000323696.5:p.Phe129Val | |
| ENST00000449224.1:c.385T>G | ENSP00000409997.1:p.Phe129Val | |
| NM_006371.4:c.385T>G , LRG_4t1:c.385T>G | NP_006362.1:p.Phe129Val | |
| NM_006371.5:c.385T>G MANE Select | NP_006362.1:p.Phe129Val | |
| NM_001393363.1:c.385T>G | NP_001380292.1:p.Phe129Val | |
| NM_001393364.1:c.385T>G | NP_001380293.1:p.Phe129Val | |
| NM_001393365.1:c.385T>G | NP_001380294.1:p.Phe129Val |