Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169586504C= , CM000663.2:g.169586504C= | GRCh38 |
| NC_000001.10:g.169555742C= , CM000663.1:g.169555742C= | GRCh37 |
| NC_000001.9:g.167822366C= | NCBI36 |
| NG_011806.1:g.5028G= , LRG_553:g.5028G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367796.3:c.-118G= | ENSP00000356770.3:n.-118G= | |
| ENST00000367797.7:c.-118G= | ENSP00000356771.3:n.-118G= | |
| NM_000130.4:c.-118G= , LRG_553t1:c.-118G= | NP_000121.2:n.-118G= | |
| XM_017000660.2:c.-437G= | XP_016856149.1:n.-437G= |