Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131860388G>T , CM000668.2:g.131860388G>T | GRCh38 |
| NC_000006.11:g.132181528G>T , CM000668.1:g.132181528G>T | GRCh37 |
| NC_000006.10:g.132223221G>T | NCBI36 |
| NG_008206.1:g.57373G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006208.3:c.797G>T MANE Select | NP_006199.2:p.Gly266Val |
| ENST00000647893.1:c.797G>T MANE Select | ENSP00000498074.1:p.Gly266Val |
| NM_006208.2:c.797G>T | NP_006199.2:p.Gly266Val |
| ENST00000360971.6:c.797G>T | ENSP00000354238.2:p.Gly266Val |
| ENST00000513998.5:c.797G>T | ENSP00000422424.1:p.Gly266Val |
| ENST00000650147.1:c.414G>T | |
| ENST00000650437.1:c.288G>T |