Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94941894T>G , CM000672.2:g.94941894T>G | GRCh38 |
| NC_000010.10:g.96701651T>G , CM000672.1:g.96701651T>G | GRCh37 |
| NC_000010.9:g.96691641T>G | NCBI36 |
| NG_008385.1:g.8237T>G | |
| NG_008385.2:g.8737T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.205T>G MANE Select | ENSP00000260682.6:p.Phe69Val | |
| ENST00000643112.1:c.205T>G | ENSP00000496202.1:p.Phe69Val | |
| ENST00000645207.1:n.358T>G | ||
| ENST00000260682.6:c.205T>G | ENSP00000260682.6:p.Phe69Val | |
| ENST00000461906.1:n.230T>G | ||
| NM_000771.3:c.205T>G | NP_000762.2:p.Phe69Val | |
| NM_000771.4:c.205T>G MANE Select | NP_000762.2:p.Phe69Val |