Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94421010G>A , CM000669.2:g.94421010G>A | GRCh38 |
| NC_000007.13:g.94050322G>A , CM000669.1:g.94050322G>A | GRCh37 |
| NC_000007.12:g.93888258G>A | NCBI36 |
| NG_007405.1:g.31450G>A , LRG_2:g.31450G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2297G>A MANE Select | NP_000080.2:p.Gly766Asp |
| ENST00000297268.11:c.2297G>A MANE Select | ENSP00000297268.6:p.Gly766Asp |
| NM_000089.3:c.2297G>A , LRG_2t1:c.2297G>A | NP_000080.2:p.Gly766Asp |
| ENST00000297268.10:c.2297G>A | ENSP00000297268.6:p.Gly766Asp |
| ENST00000461525.5:n.386G>A | |
| ENST00000467931.1:n.677G>A | |
| ENST00000473573.5:n.634G>A | |
| ENST00000497316.5:n.694G>A | |
| ENST00000620463.1:c.2291G>A | ENSP00000477719.1:p.Gly764Asp |