Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.49951169C= , CM000674.2:g.49951169C= | GRCh38 |
| NC_000012.11:g.50344952C= , CM000674.1:g.50344952C= | GRCh37 |
| NC_000012.10:g.48631219C= | NCBI36 |
| NG_008913.1:g.5429C= , LRG_717:g.5429C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000199280.4:c.339C= MANE Select | ENSP00000199280.3:p.Arg113= | |
| ENST00000199280.3:c.339C= | ENSP00000199280.3:p.Arg113= | |
| ENST00000550862.1:c.339C= | ENSP00000450022.1:p.Arg113= | |
| ENST00000551526.5:c.339C= | ENSP00000447148.1:p.Arg113= | |
| NM_000486.5:c.339C= , LRG_717t1:c.339C= | NP_000477.1:p.Arg113= | |
| NM_000486.6:c.339C= MANE Select | NP_000477.1:p.Arg113= |