Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.124869057G>T , CM000673.2:g.124869057G>T | GRCh38 |
| NC_000011.9:g.124738953G>T , CM000673.1:g.124738953G>T | GRCh37 |
| NC_000011.8:g.124244163G>T | NCBI36 |
| NG_016214.1:g.8649G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_022370.4:c.416G>T MANE Select | NP_071765.2:p.Gly139Val |
| ENST00000397801.6:c.416G>T MANE Select | ENSP00000380903.1:p.Gly139Val |
| NM_022370.3:c.416G>T | NP_071765.2:p.Gly139Val |
| ENST00000397801.5:c.416G>T | ENSP00000380903.1:p.Gly139Val |
| ENST00000538940.5:c.350G>T | ENSP00000441797.1:p.Gly117Val |
| XM_011542953.1:c.1388G>T | XP_011541255.1:p.Gly463Val |
| XM_017018122.1:c.350G>T | XP_016873611.1:p.Gly117Val |