Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67584706T>G , CM000673.2:g.67584706T>G | GRCh38 |
| NC_000011.9:g.67352177T>G , CM000673.1:g.67352177T>G | GRCh37 |
| NC_000011.8:g.67108753T>G | NCBI36 |
| NG_012075.1:g.6112T>G , LRG_723:g.6112T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.166T>G | ENSP00000381604.1:p.Phe56Val | |
| ENST00000398606.10:c.166T>G MANE Select | ENSP00000381607.3:p.Phe56Val | |
| ENST00000646888.1:c.59T>G | ENSP00000494477.1:p.Val20Gly | |
| ENST00000398603.5:c.166T>G | ENSP00000381604.1:p.Phe56Val | |
| ENST00000398606.7:c.166T>G | ENSP00000381607.3:p.Phe56Val | |
| ENST00000489040.1:n.165T>G | ||
| ENST00000494593.1:n.596T>G | ||
| ENST00000498765.5:c.129T>G | ||
| NM_000852.3:c.166T>G , LRG_723t1:c.166T>G | NP_000843.1:p.Phe56Val | |
| NM_000852.4:c.166T>G MANE Select | NP_000843.1:p.Phe56Val |