Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94419507G>A , CM000669.2:g.94419507G>A | GRCh38 |
| NC_000007.13:g.94048819G>A , CM000669.1:g.94048819G>A | GRCh37 |
| NC_000007.12:g.93886755G>A | NCBI36 |
| NG_007405.1:g.29947G>A , LRG_2:g.29947G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.2035G>A MANE Select | NP_000080.2:p.Gly679Ser |
| ENST00000297268.11:c.2035G>A MANE Select | ENSP00000297268.6:p.Gly679Ser |
| NM_000089.3:c.2035G>A , LRG_2t1:c.2035G>A | NP_000080.2:p.Gly679Ser |
| ENST00000297268.10:c.2035G>A | ENSP00000297268.6:p.Gly679Ser |
| ENST00000461525.5:n.124G>A | |
| ENST00000467931.1:n.55G>A | |
| ENST00000473573.5:n.372G>A | |
| ENST00000497316.5:n.432G>A | |
| ENST00000620463.1:c.2029G>A | ENSP00000477719.1:p.Gly677Ser |