Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862757C= , CM000666.2:g.4862757C= | GRCh38 |
| NC_000004.11:g.4864484C= , CM000666.1:g.4864484C= | GRCh37 |
| NC_000004.10:g.4915385C= | NCBI36 |
| NG_008121.1:g.8093C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.526C= MANE Select | ENSP00000372170.4:p.Arg176= | |
| ENST00000382723.4:c.526C= | ENSP00000372170.4:p.Arg176= | |
| ENST00000468421.1:n.238C= | ||
| NM_002448.3:c.526C= MANE Select | NP_002439.2:p.Arg176= |