Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2277867G>C , CM000678.2:g.2277867G>C | GRCh38 |
| NC_000016.9:g.2327868G>C , CM000678.1:g.2327868G>C | GRCh37 |
| NC_000016.8:g.2267869G>C | NCBI36 |
| NG_011790.1:g.67880C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001089.3:c.4909+12C>G MANE Select | NP_001080.2:n.4909+12C>G |
| ENST00000301732.10:c.4909+12C>G MANE Select | ENSP00000301732.5:n.4909+12C>G |
| NM_001089.2:c.4909+12C>G | NP_001080.2:n.4909+12C>G |
| ENST00000301732.9:c.4909+12C>G | ENSP00000301732.5:n.4909+12C>G |
| ENST00000382381.7:c.4735+12C>G | ENSP00000371818.3:n.4735+12C>G |