Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989063C>G , CM000672.2:g.94989063C>G | GRCh38 |
| NC_000010.10:g.96748820C>G , CM000672.1:g.96748820C>G | GRCh37 |
| NC_000010.9:g.96738810C>G | NCBI36 |
| NG_008385.1:g.55406C>G | |
| NG_008385.2:g.55906C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.*35C>G MANE Select | ENSP00000260682.6:n.*35C>G | |
| ENST00000643112.1:c.*517C>G | ENSP00000496202.1:n.*517C>G | |
| ENST00000260682.6:c.*35C>G | ENSP00000260682.6:n.*35C>G | |
| NM_000771.3:c.*35C>G | NP_000762.2:n.*35C>G | |
| NM_000771.4:c.*35C>G MANE Select | NP_000762.2:n.*35C>G |