Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800087G>A , CM000666.2:g.24800087G>A | GRCh38 |
| NC_000004.11:g.24801709G>A , CM000666.1:g.24801709G>A | GRCh37 |
| NC_000004.10:g.24410807G>A | NCBI36 |
| NG_012213.1:g.9625G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.566G>A MANE Select | ENSP00000371554.3:p.Arg189His | |
| ENST00000382120.3:c.566G>A | ENSP00000371554.3:p.Arg189His | |
| NM_003102.2:c.566G>A | NP_003093.2:p.Arg189His | |
| XR_427488.1:n.756G>A | ||
| NM_003102.3:c.566G>A | NP_003093.2:p.Arg189His | |
| NM_003102.4:c.566G>A MANE Select | NP_003093.2:p.Arg189His |