| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92609383A>G , CM000672.2:g.92609383A>G | GRCh38 |
| NC_000010.10:g.94369140A>G , CM000672.1:g.94369140A>G | GRCh37 |
| NC_000010.9:g.94359120A>G | NCBI36 |
| NG_032580.1:g.21316A>G |
| HGVS | Amino-acid Change |
|---|---|
| NM_004523.4:c.574-2A>G MANE Select | NP_004514.2:n.574-2A>G |
| ENST00000260731.5:c.574-2A>G MANE Select | ENSP00000260731.3:n.574-2A>G |
| NM_004523.3:c.574-2A>G | NP_004514.2:n.574-2A>G |
| ENST00000260731.4:c.574-2A>G | ENSP00000260731.3:n.574-2A>G |
| ENST00000676621.1:c.574-2A>G | ENSP00000503639.1:n.574-2A>G |
| ENST00000676647.1:c.367-2A>G | ENSP00000503394.1:n.367-2A>G |
| ENST00000676757.1:c.367-2A>G | ENSP00000504289.1:n.367-2A>G |
| ENST00000677720.1:c.574-2A>G | ENSP00000504840.1:n.574-2A>G |