Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989134C= , CM000672.2:g.94989134C= | GRCh38 |
| NC_000010.10:g.96748891C= , CM000672.1:g.96748891C= | GRCh37 |
| NC_000010.9:g.96738881C= | NCBI36 |
| NG_008385.1:g.55477C= | |
| NG_008385.2:g.55977C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.*106C= MANE Select | ENSP00000260682.6:n.*106C= | |
| ENST00000643112.1:c.*588C= | ENSP00000496202.1:n.*588C= | |
| ENST00000260682.6:c.*106C= | ENSP00000260682.6:n.*106C= | |
| NM_000771.3:c.*106C= | NP_000762.2:n.*106C= | |
| NM_000771.4:c.*106C= MANE Select | NP_000762.2:n.*106C= |