Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92613482A>G , CM000672.2:g.92613482A>G | GRCh38 |
| NC_000010.10:g.94373239A>G , CM000672.1:g.94373239A>G | GRCh37 |
| NC_000010.9:g.94363219A>G | NCBI36 |
| NG_032580.1:g.25415A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260731.5:c.895A>G MANE Select | ENSP00000260731.3:p.Ile299Val | |
| ENST00000676621.1:c.895A>G | ENSP00000503639.1:p.Ile299Val | |
| ENST00000676647.1:c.688A>G | ENSP00000503394.1:p.Ile230Val | |
| ENST00000676757.1:c.688A>G | ENSP00000504289.1:p.Ile230Val | |
| ENST00000677720.1:c.895A>G | ENSP00000504840.1:p.Ile299Val | |
| ENST00000260731.4:c.895A>G | ENSP00000260731.3:p.Ile299Val | |
| NM_004523.3:c.895A>G | NP_004514.2:p.Ile299Val | |
| NM_004523.4:c.895A>G MANE Select | NP_004514.2:p.Ile299Val |