Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94007707T= , CM000663.2:g.94007707T= | GRCh38 |
| NC_000001.10:g.94473263T= , CM000663.1:g.94473263T= | GRCh37 |
| NC_000001.9:g.94245851T= | NCBI36 |
| NG_009073.1:g.118443A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.5932A= MANE Select | NP_000341.2:p.Lys1978= |
| ENST00000370225.4:c.5932A= MANE Select | ENSP00000359245.3:p.Lys1978= |
| NM_000350.2:c.5932A= | NP_000341.2:p.Lys1978= |
| ENST00000370225.3:c.5932A= | ENSP00000359245.3:p.Lys1978= |
| ENST00000465352.1:n.348A= | |
| ENST00000484388.1:n.46A= | |
| ENST00000536513.5:c.2308A= | ENSP00000439707.2:p.Lys770= |