Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3083037C= , CM000682.2:g.3083037C= | GRCh38 |
| NC_000020.10:g.3063683C= , CM000682.1:g.3063683C= | GRCh37 |
| NC_000020.9:g.3011683C= | NCBI36 |
| NG_008663.1:g.6688G= , LRG_715:g.6688G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000490.5:c.262G= MANE Select | NP_000481.2:p.Gly88= |
| ENST00000380293.3:c.262G= MANE Select | ENSP00000369647.3:p.Gly88= |
| NM_000490.4:c.262G= , LRG_715t1:c.262G= | NP_000481.2:p.Gly88= |
| XM_011529267.1:c.262G= | XP_011527569.1:p.Gly88= |
| XM_011529267.2:c.262G= | XP_011527569.1:p.Gly88= |