Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94948989C>G , CM000672.2:g.94948989C>G | GRCh38 |
| NC_000010.10:g.96708746C>G , CM000672.1:g.96708746C>G | GRCh37 |
| NC_000010.9:g.96698736C>G | NCBI36 |
| NG_008385.1:g.15332C>G | |
| NG_008385.2:g.15832C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.643-119C>G MANE Select | ENSP00000260682.6:n.643-119C>G | |
| ENST00000643112.1:c.643-119C>G | ENSP00000496202.1:n.643-119C>G | |
| ENST00000260682.6:c.643-119C>G | ENSP00000260682.6:n.643-119C>G | |
| ENST00000473496.1:n.414-119C>G | ||
| NM_000771.3:c.643-119C>G | NP_000762.2:n.643-119C>G | |
| NM_000771.4:c.643-119C>G MANE Select | NP_000762.2:n.643-119C>G |