Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66560447G>T , CM000673.2:g.66560447G>T | GRCh38 |
| NC_000011.9:g.66327918G>T , CM000673.1:g.66327918G>T | GRCh37 |
| NC_000011.8:g.66084494G>T | NCBI36 |
| NG_013304.2:g.18528G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000513398.2:c.1678-126G>T MANE Select | ENSP00000426797.1:n.1678-126G>T | |
| ENST00000502692.5:c.1807-126G>T | ENSP00000422007.1:n.1807-126G>T | |
| ENST00000513398.1:c.1678-126G>T | ENSP00000426797.1:n.1678-126G>T | |
| NM_001104.3:c.1678-126G>T | NP_001095.2:n.1678-126G>T | |
| NM_001258371.2:c.1807-126G>T | NP_001245300.2:n.1807-126G>T | |
| NM_001104.4:c.1678-126G>T MANE Select | NP_001095.2:n.1678-126G>T | |
| NM_001258371.3:c.1807-126G>T | NP_001245300.2:n.1807-126G>T |