Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928853C>G , CM000684.2:g.43928853C>G | GRCh38 |
| NC_000022.10:g.44324733C>G , CM000684.1:g.44324733C>G | GRCh37 |
| NC_000022.9:g.42656066C>G | NCBI36 |
| NG_008631.1:g.10115C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.450C>G MANE Select | ENSP00000216180.3:p.Phe150Leu | |
| ENST00000216180.7:c.450C>G | ENSP00000216180.3:p.Phe150Leu | |
| ENST00000406117.6:c.*82C>G | ENSP00000384668.2:n.*82C>G | |
| ENST00000423180.2:c.438C>G | ENSP00000397987.2:p.Phe146Leu | |
| ENST00000478713.1:n.484C>G | ||
| NM_025225.2:c.450C>G | NP_079501.2:p.Phe150Leu | |
| NM_025225.3:c.450C>G MANE Select | NP_079501.2:p.Phe150Leu |