Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154781C= , CM000681.2:g.55154781C= | GRCh38 |
| NC_000019.9:g.55666149C= , CM000681.1:g.55666149C= | GRCh37 |
| NC_000019.8:g.60357961C= | NCBI36 |
| NG_007866.2:g.7952G= , LRG_432:g.7952G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.332G= MANE Select | ENSP00000341838.5:p.Arg111= | |
| ENST00000665070.1:c.332G= | ENSP00000499482.1:p.Arg111= | |
| ENST00000344887.9:c.332G= | ENSP00000341838.5:p.Arg111= | |
| ENST00000585806.5:n.331G= | ||
| ENST00000586669.5:n.340G= | ||
| ENST00000587176.5:n.516G= | ||
| ENST00000587871.1:c.951G= | ||
| ENST00000588882.1:c.257G= | ENSP00000466729.1:p.Arg86= | |
| ENST00000590463.1:n.504G= | ||
| NM_000363.4:c.332G= , LRG_432t1:c.332G= | NP_000354.4:p.Arg111= | |
| NM_000363.5:c.332G= MANE Select | NP_000354.4:p.Arg111= |