Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.76718494G>A , CM000667.2:g.76718494G>A | GRCh38 |
| NC_000005.9:g.76014319G>A , CM000667.1:g.76014319G>A | GRCh37 |
| NC_000005.8:g.76050075G>A | NCBI36 |
| NG_032906.1:g.7452G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001992.5:c.88+2099G>A MANE Select | NP_001983.2:n.88+2099G>A |
| ENST00000319211.5:c.88+2099G>A MANE Select | ENSP00000321326.4:n.88+2099G>A |
| NM_001311313.1:c.-398+2099G>A | NP_001298242.1:n.-398+2099G>A |
| NM_001311313.2:c.-398+2099G>A | NP_001298242.1:n.-398+2099G>A |
| NM_001992.3:c.88+2099G>A | NP_001983.2:n.88+2099G>A |
| NM_001992.4:c.88+2099G>A | NP_001983.2:n.88+2099G>A |
| ENST00000319211.4:c.88+2099G>A | ENSP00000321326.4:n.88+2099G>A |