Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154145C= , CM000681.2:g.55154145C= | GRCh38 |
| NC_000019.9:g.55665513C= , CM000681.1:g.55665513C= | GRCh37 |
| NC_000019.8:g.60357325C= | NCBI36 |
| NG_007866.2:g.8588G= , LRG_432:g.8588G= | |
| NG_011829.2:g.94G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.434G= MANE Select | NP_000354.4:p.Arg145= |
| ENST00000344887.10:c.434G= MANE Select | ENSP00000341838.5:p.Arg145= |
| NM_000363.4:c.434G= , LRG_432t1:c.434G= | NP_000354.4:p.Arg145= |
| ENST00000344887.9:c.434G= | ENSP00000341838.5:p.Arg145= |
| ENST00000585806.5:n.433G= | |
| ENST00000586669.5:n.442G= | |
| ENST00000588882.1:c.359G= | ENSP00000466729.1:p.Arg120= |
| ENST00000589864.1:n.262G= | |
| ENST00000665070.1:c.467G= | ENSP00000499482.1:p.Arg156= |