Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10612472A= , CM000670.2:g.10612472A= | GRCh38 |
| NC_000008.10:g.10469982A= , CM000670.1:g.10469982A= | GRCh37 |
| NC_000008.9:g.10507392A= | NCBI36 |
| NG_028035.1:g.47636T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.1626T= MANE Select | ENSP00000371923.3:p.His542= | |
| ENST00000382483.3:c.1626T= | ENSP00000371923.3:p.His542= | |
| NM_178857.5:c.1626T= | NP_849188.4:p.His542= | |
| NM_178857.6:c.1626T= MANE Select | NP_849188.4:p.His542= |