Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.129818837A= , CM000671.2:g.129818837A= | GRCh38 |
| NC_000009.11:g.132581116A= , CM000671.1:g.132581116A= | GRCh37 |
| NC_000009.10:g.131620937A= | NCBI36 |
| NG_008049.1:g.10326T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000351698.5:c.528T= MANE Select | ENSP00000345719.4:p.His176= | |
| ENST00000651202.1:c.624T= | ENSP00000498222.1:p.His208= | |
| ENST00000351698.4:c.528T= | ENSP00000345719.4:p.His176= | |
| ENST00000473604.2:n.638T= | ||
| NM_000113.2:c.528T= | NP_000104.1:p.His176= | |
| XR_929731.1:n.688T= | ||
| XR_929731.3:n.556T= | ||
| NM_000113.3:c.528T= MANE Select | NP_000104.1:p.His176= |