Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31593017T= , CM000680.2:g.31593017T= | GRCh38 |
| NC_000018.9:g.29172980T= , CM000680.1:g.29172980T= | GRCh37 |
| NC_000018.8:g.27426978T= | NCBI36 |
| NG_009490.1:g.6251T= , LRG_416:g.6251T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000371.4:c.191T= MANE Select | NP_000362.1:p.Phe64= |
| ENST00000237014.8:c.191T= MANE Select | ENSP00000237014.4:p.Phe64= |
| NM_000371.3:c.191T= , LRG_416t1:c.191T= | NP_000362.1:p.Phe64= |
| ENST00000237014.7:c.191T= | ENSP00000237014.3:p.Phe64= |
| ENST00000432547.7:n.217T= | |
| ENST00000541025.2:n.217T= | |
| ENST00000610404.4:c.191T= | ENSP00000477599.1:p.Phe64= |
| ENST00000610404.5:c.95T= | ENSP00000477599.2:p.Phe32= |
| ENST00000613781.1:c.191T= | ENSP00000479174.1:p.Phe64= |
| ENST00000649620.1:c.191T= | ENSP00000497927.1:p.Phe64= |