Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189066461C= , CM000664.2:g.189066461C= | GRCh38 |
| NC_000002.11:g.189931187C= , CM000664.1:g.189931187C= | GRCh37 |
| NC_000002.10:g.189639432C= | NCBI36 |
| NG_011799.1:g.118419G= | |
| NG_011799.2:g.118419G= | |
| NG_011799.3:g.163841G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000393.5:c.1492G= MANE Select | NP_000384.2:p.Gly498= |
| ENST00000374866.9:c.1492G= MANE Select | ENSP00000364000.3:p.Gly498= |
| NM_000393.3:c.1492G= | NP_000384.2:p.Gly498= |
| NM_000393.4:c.1492G= | NP_000384.2:p.Gly498= |
| ENST00000374866.7:c.1492G= | ENSP00000364000.3:p.Gly498= |
| ENST00000618828.1:c.359-28G= | ENSP00000482184.1:n.359-28G= |
| XM_011510573.1:c.1354G= | XP_011508875.1:p.Gly452= |
| XM_011510573.3:c.1354G= | XP_011508875.1:p.Gly452= |