Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44288455T= , CM000683.2:g.44288455T= | GRCh38 |
| NC_000021.8:g.45708338T= , CM000683.1:g.45708338T= | GRCh37 |
| NC_000021.7:g.44532766T= | NCBI36 |
| NG_009556.1:g.7576T= , LRG_18:g.7576T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.649T= MANE Select | ENSP00000291582.5:p.Ser217= | |
| ENST00000291582.5:c.649T= | ENSP00000291582.5:p.Ser217= | |
| ENST00000527919.5:n.1193T= | ||
| ENST00000530812.5:n.1201T= | ||
| NM_000383.3:c.649T= | NP_000374.1:p.Ser217= | |
| XM_011529551.1:c.649T= | XP_011527853.1:p.Ser217= | |
| NM_000383.4:c.649T= MANE Select | NP_000374.1:p.Ser217= |