Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.3082860G= , CM000682.2:g.3082860G= | GRCh38 |
| NC_000020.10:g.3063506G= , CM000682.1:g.3063506G= | GRCh37 |
| NC_000020.9:g.3011506G= | NCBI36 |
| NG_008663.1:g.6865C= , LRG_715:g.6865C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380293.3:c.323-58C= MANE Select | ENSP00000369647.3:n.323-58C= | |
| NM_000490.4:c.323-58C= , LRG_715t1:c.323-58C= | NP_000481.2:n.323-58C= | |
| XM_011529267.1:c.323-58C= | XP_011527569.1:n.323-58C= | |
| XM_011529267.2:c.323-58C= | XP_011527569.1:n.323-58C= | |
| NM_000490.5:c.323-58C= MANE Select | NP_000481.2:n.323-58C= |