Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115717869A= , CM000663.2:g.115717869A= | GRCh38 |
| NC_000001.10:g.116260490A= , CM000663.1:g.116260490A= | GRCh37 |
| NC_000001.9:g.116062013A= | NCBI36 |
| NG_008802.1:g.55937T= , LRG_404:g.55937T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001232.4:c.809T= MANE Select | NP_001223.2:p.Ile270= |
| ENST00000261448.6:c.809T= MANE Select | ENSP00000261448.5:p.Ile270= |
| NM_001232.3:c.809T= , LRG_404t1:c.809T= | NP_001223.2:p.Ile270= |
| ENST00000261448.5:c.809T= | ENSP00000261448.5:p.Ile270= |
| ENST00000488931.2:c.*181T= | ENSP00000518226.1:n.*181T= |