Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4862704G= , CM000666.2:g.4862704G= | GRCh38 |
| NC_000004.11:g.4864431G= , CM000666.1:g.4864431G= | GRCh37 |
| NC_000004.10:g.4915332G= | NCBI36 |
| NG_008121.1:g.8040G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.473G= MANE Select | ENSP00000372170.4:p.Arg158= | |
| ENST00000382723.4:c.473G= | ENSP00000372170.4:p.Arg158= | |
| ENST00000468421.1:n.185G= | ||
| NM_002448.3:c.473G= MANE Select | NP_002439.2:p.Arg158= |