Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.20618562C= , CM000663.2:g.20618562C= | GRCh38 |
| NC_000001.10:g.20945055C= , CM000663.1:g.20945055C= | GRCh37 |
| NC_000001.9:g.20817642C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375071.4:c.435C= MANE Select | ENSP00000364212.3:p.Thr145= | |
| ENST00000375071.3:c.435C= | ENSP00000364212.3:p.Thr145= | |
| ENST00000461985.1:n.421C= | ||
| NM_001785.2:c.435C= | NP_001776.1:p.Thr145= | |
| NM_001785.3:c.435C= MANE Select | NP_001776.1:p.Thr145= |