Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55156207C= , CM000681.2:g.55156207C= | GRCh38 |
| NC_000019.9:g.55667575C= , CM000681.1:g.55667575C= | GRCh37 |
| NC_000019.8:g.60359387C= | NCBI36 |
| NG_007866.2:g.6526G= , LRG_432:g.6526G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.276G= MANE Select | ENSP00000341838.5:p.Glu92= | |
| ENST00000665070.1:c.276G= | ENSP00000499482.1:p.Glu92= | |
| ENST00000344887.9:c.276G= | ENSP00000341838.5:p.Glu92= | |
| ENST00000585806.5:n.275G= | ||
| ENST00000586669.5:n.284G= | ||
| ENST00000587176.5:n.460G= | ||
| ENST00000587871.1:c.895G= | ||
| ENST00000588882.1:c.201G= | ENSP00000466729.1:p.Glu67= | |
| ENST00000590463.1:n.448G= | ||
| NM_000363.4:c.276G= , LRG_432t1:c.276G= | NP_000354.4:p.Glu92= | |
| NM_000363.5:c.276G= MANE Select | NP_000354.4:p.Glu92= |