Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57766047G= , CM000674.2:g.57766047G= | GRCh38 |
| NC_000012.11:g.58159830G= , CM000674.1:g.58159830G= | GRCh37 |
| NC_000012.10:g.56446097G= | NCBI36 |
| NG_007076.1:g.6147C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000546609.2:n.258C= | ||
| ENST00000713544.1:c.346C= | ENSP00000518840.1:p.His116= | |
| ENST00000713545.1:c.346C= | ENSP00000518841.1:p.His116= | |
| ENST00000228606.9:c.346C= MANE Select | ENSP00000228606.4:p.His116= | |
| ENST00000228606.8:c.346C= | ENSP00000228606.4:p.His116= | |
| ENST00000546496.1:n.174C= | ||
| ENST00000546609.1:c.258C= | ||
| ENST00000547344.5:n.400C= | ||
| ENST00000552186.1:n.465C= | ||
| NM_000785.3:c.346C= | NP_000776.1:p.His116= | |
| NM_000785.4:c.346C= MANE Select | NP_000776.1:p.His116= |