Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154806G= , CM000681.2:g.55154806G= | GRCh38 |
| NC_000019.9:g.55666174G= , CM000681.1:g.55666174G= | GRCh37 |
| NC_000019.8:g.60357986G= | NCBI36 |
| NG_007866.2:g.7927C= , LRG_432:g.7927C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.307C= MANE Select | NP_000354.4:p.Arg103= |
| ENST00000344887.10:c.307C= MANE Select | ENSP00000341838.5:p.Arg103= |
| NM_000363.4:c.307C= , LRG_432t1:c.307C= | NP_000354.4:p.Arg103= |
| ENST00000344887.9:c.307C= | ENSP00000341838.5:p.Arg103= |
| ENST00000585806.5:n.306C= | |
| ENST00000586669.5:n.315C= | |
| ENST00000587176.5:n.491C= | |
| ENST00000587871.1:c.926C= | |
| ENST00000588882.1:c.232C= | ENSP00000466729.1:p.Arg78= |
| ENST00000590463.1:n.479C= | |
| ENST00000665070.1:c.307C= | ENSP00000499482.1:p.Arg103= |