Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121627041C= , CM000674.2:g.121627041C= | GRCh38 |
| NC_000012.11:g.122064947C= , CM000674.1:g.122064947C= | GRCh37 |
| NC_000012.10:g.120549330C= | NCBI36 |
| NG_007500.1:g.5467C= , LRG_93:g.5467C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698901.1:n.425+108C= | ||
| ENST00000617316.2:c.294C= | ENSP00000482568.2:p.Gly98= | |
| ENST00000646827.1:n.492C= | ||
| ENST00000611718.1:c.105C= | ENSP00000477953.1:p.Gly35= | |
| ENST00000616379.1:c.294C= | ENSP00000480616.1:p.Gly98= | |
| ENST00000617316.1:c.105C= | ENSP00000482568.1:p.Gly35= | |
| NM_032790.3:c.294C= , LRG_93t1:c.294C= | NP_116179.2:p.Gly98= |