Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52033589T= , CM000666.2:g.52033589T= | GRCh38 |
| NC_000004.11:g.52899755T= , CM000666.1:g.52899755T= | GRCh37 |
| NC_000004.10:g.52594512T= | NCBI36 |
| NG_008891.1:g.9731A= , LRG_204:g.9731A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000232.5:c.85A= MANE Select | NP_000223.1:p.Arg29= |
| ENST00000381431.10:c.85A= MANE Select | ENSP00000370839.6:p.Arg29= |
| NM_000232.4:c.85A= , LRG_204t1:c.85A= | NP_000223.1:p.Arg29= |
| ENST00000381431.9:c.85A= | ENSP00000370839.5:p.Arg29= |
| ENST00000506357.5:c.71A= | |
| ENST00000514133.1:c.52A= | ENSP00000425818.1:p.Arg18= |
| XM_011534403.1:c.34-3726A= | XP_011532705.1:n.34-3726A= |