Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94989069A>G , CM000672.2:g.94989069A>G | GRCh38 |
| NC_000010.10:g.96748826A>G , CM000672.1:g.96748826A>G | GRCh37 |
| NC_000010.9:g.96738816A>G | NCBI36 |
| NG_008385.1:g.55412A>G | |
| NG_008385.2:g.55912A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.*41A>G MANE Select | ENSP00000260682.6:n.*41A>G | |
| ENST00000643112.1:c.*523A>G | ENSP00000496202.1:n.*523A>G | |
| ENST00000260682.6:c.*41A>G | ENSP00000260682.6:n.*41A>G | |
| NM_000771.3:c.*41A>G | NP_000762.2:n.*41A>G | |
| NM_000771.4:c.*41A>G MANE Select | NP_000762.2:n.*41A>G |