Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56929515A>G , CM000674.2:g.56929515A>G | GRCh38 |
| NC_000012.11:g.57323299A>G , CM000674.1:g.57323299A>G | GRCh37 |
| NC_000012.10:g.55609566A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_148897.3:c.599T>C MANE Select | NP_683695.1:p.Ile200Thr |
| ENST00000293502.2:c.599T>C MANE Select | ENSP00000293502.1:p.Ile200Thr |
| NM_148897.2:c.599T>C | NP_683695.1:p.Ile200Thr |
| ENST00000293502.1:c.599T>C | ENSP00000293502.1:p.Ile200Thr |