Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42901099T>G , CM000679.2:g.42901099T>G | GRCh38 |
| NC_000017.10:g.41053116T>G , CM000679.1:g.41053116T>G | GRCh37 |
| NC_000017.9:g.38306642T>G | NCBI36 |
| NG_011808.1:g.5302T>G , LRG_147:g.5302T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.223T>G MANE Select | ENSP00000253801.1:p.Phe75Val | |
| ENST00000253801.6:c.223T>G | ENSP00000253801.1:p.Phe75Val | |
| ENST00000585489.1:c.223T>G | ENSP00000466202.1:p.Phe75Val | |
| ENST00000588481.1:n.288T>G | ||
| ENST00000592383.5:c.223T>G | ENSP00000465958.1:p.Phe75Val | |
| NM_000151.3:c.223T>G | NP_000142.2:p.Phe75Val | |
| NM_001270397.1:c.223T>G | NP_001257326.1:p.Phe75Val | |
| NM_000151.4:c.223T>G MANE Select | NP_000142.2:p.Phe75Val | |
| NM_001270397.2:c.223T>G | NP_001257326.1:p.Phe75Val |