Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021665T= , CM000663.2:g.94021665T= | GRCh38 |
| NC_000001.10:g.94487221T= , CM000663.1:g.94487221T= | GRCh37 |
| NC_000001.9:g.94259809T= | NCBI36 |
| NG_009073.1:g.104485A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4823A= MANE Select | ENSP00000359245.3:p.His1608= | |
| ENST00000370225.3:c.4823A= | ENSP00000359245.3:p.His1608= | |
| ENST00000460514.1:n.317A= | ||
| ENST00000536513.5:c.1199A= | ENSP00000439707.2:p.His400= | |
| NM_000350.2:c.4823A= | NP_000341.2:p.His1608= | |
| NM_000350.3:c.4823A= MANE Select | NP_000341.2:p.His1608= |