Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94418518G>T , CM000669.2:g.94418518G>T | GRCh38 |
| NC_000007.13:g.94047830G>T , CM000669.1:g.94047830G>T | GRCh37 |
| NC_000007.12:g.93885766G>T | NCBI36 |
| NG_007405.1:g.28958G>T , LRG_2:g.28958G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.1991G>T MANE Select | NP_000080.2:p.Gly664Val |
| ENST00000297268.11:c.1991G>T MANE Select | ENSP00000297268.6:p.Gly664Val |
| NM_000089.3:c.1991G>T , LRG_2t1:c.1991G>T | NP_000080.2:p.Gly664Val |
| ENST00000297268.10:c.1991G>T | ENSP00000297268.6:p.Gly664Val |
| ENST00000461525.5:n.80G>T | |
| ENST00000473573.5:n.328G>T | |
| ENST00000497316.5:n.388G>T | |
| ENST00000620463.1:c.1985G>T | ENSP00000477719.1:p.Gly662Val |