Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33060846C>A , CM000675.2:g.33060846C>A | GRCh38 |
| NC_000013.10:g.33634983C>A , CM000675.1:g.33634983C>A | GRCh37 |
| NC_000013.9:g.32532983C>A | NCBI36 |
| NG_011485.1:g.49413C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004795.4:c.1767C>A MANE Select | NP_004786.2:p.His589Gln |
| ENST00000380099.4:c.1767C>A MANE Select | ENSP00000369442.3:p.His589Gln |
| NM_004795.3:c.1767C>A | NP_004786.2:p.His589Gln |
| ENST00000380099.3:c.1767C>A | ENSP00000369442.3:p.His589Gln |
| ENST00000487852.1:n.1825C>A | |
| XM_006719895.1:c.846C>A | XP_006719958.1:p.His282Gln |
| XM_006719895.2:c.846C>A | XP_006719958.1:p.His282Gln |