Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169707345A= , CM000663.2:g.169707345A= | GRCh38 |
| NC_000001.10:g.169676486A= , CM000663.1:g.169676486A= | GRCh37 |
| NC_000001.9:g.167943110A= | NCBI36 |
| NG_016132.1:g.9358T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000655.5:c.577T= (SELL) MANE Select | NP_000646.3:p.Phe193= |
| ENST00000236147.6:c.577T= (SELL) MANE Select | ENSP00000236147.5:p.Phe193= |
| NM_000655.4:c.616T= (SELL) | NP_000646.2:p.Phe206= |
| NR_029467.1:n.545T= (SELL) | |
| NR_029467.2:n.546T= (SELL) | |
| ENST00000236147.4:c.616T= (SELL) | ENSP00000236147.4:p.Phe206= |
| ENST00000463108.5:n.777T= (SELL) | |
| ENST00000466340.1:n.589T= (SELL) | |
| ENST00000479657.5:n.329T= (SELL) | |
| ENST00000498289.5:n.851+23413A= (FIRRM) | |
| ENST00000650983.1:c.616T= (SELL) | ENSP00000498227.1:p.Phe206= |