Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57762420G>C , CM000674.2:g.57762420G>C | GRCh38 |
| NC_000012.11:g.58156203G>C , CM000674.1:g.58156203G>C | GRCh37 |
| NC_000012.10:g.56442470G>C | NCBI36 |
| NG_007076.1:g.9774C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.*722C>G | ENSP00000518840.1:n.*722C>G | |
| ENST00000713545.1:c.*1254C>G | ENSP00000518841.1:n.*1254C>G | |
| ENST00000228606.9:c.*722C>G MANE Select | ENSP00000228606.4:n.*722C>G | |
| ENST00000228606.8:c.*722C>G | ENSP00000228606.4:n.*722C>G | |
| ENST00000547344.5:n.2388C>G | ||
| NM_000785.3:c.*722C>G | NP_000776.1:n.*722C>G | |
| NM_000785.4:c.*722C>G MANE Select | NP_000776.1:n.*722C>G |