Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.173232745C>T , CM000667.2:g.173232745C>T | GRCh38 |
| NC_000005.9:g.172659748C>T , CM000667.1:g.172659748C>T | GRCh37 |
| NC_000005.8:g.172592354C>T | NCBI36 |
| NG_013340.1:g.7568G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004387.4:c.799G>A MANE Select | NP_004378.1:p.Gly267Ser |
| ENST00000329198.5:c.799G>A MANE Select | ENSP00000327758.4:p.Gly267Ser |
| NM_001166175.1:c.*752G>A | NP_001159647.1:n.*752G>A |
| NM_001166175.2:c.*752G>A | NP_001159647.1:n.*752G>A |
| NM_001166176.1:c.*598G>A | NP_001159648.1:n.*598G>A |
| NM_001166176.2:c.*598G>A | NP_001159648.1:n.*598G>A |
| NM_004387.3:c.799G>A | NP_004378.1:p.Gly267Ser |
| ENST00000329198.4:c.799G>A | ENSP00000327758.4:p.Gly267Ser |