Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55151881C= , CM000681.2:g.55151881C= | GRCh38 |
| NC_000019.9:g.55663249C= , CM000681.1:g.55663249C= | GRCh37 |
| NC_000019.8:g.60355061C= | NCBI36 |
| NG_007866.2:g.10852G= , LRG_432:g.10852G= | |
| NG_011829.2:g.2358G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.586G= MANE Select | NP_000354.4:p.Asp196= |
| ENST00000344887.10:c.586G= MANE Select | ENSP00000341838.5:p.Asp196= |
| NM_000363.4:c.586G= , LRG_432t1:c.586G= | NP_000354.4:p.Asp196= |
| ENST00000344887.9:c.586G= | ENSP00000341838.5:p.Asp196= |
| ENST00000585806.5:n.585G= | |
| ENST00000588882.1:c.511G= | ENSP00000466729.1:p.Asp171= |
| ENST00000589864.1:n.414G= | |
| ENST00000665070.1:c.619G= | ENSP00000499482.1:p.Asp207= |