Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94411128G>A , CM000669.2:g.94411128G>A | GRCh38 |
| NC_000007.13:g.94040440G>A , CM000669.1:g.94040440G>A | GRCh37 |
| NC_000007.12:g.93878376G>A | NCBI36 |
| NG_007405.1:g.21568G>A , LRG_2:g.21568G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.1324G>A MANE Select | NP_000080.2:p.Gly442Arg |
| ENST00000297268.11:c.1324G>A MANE Select | ENSP00000297268.6:p.Gly442Arg |
| NM_000089.3:c.1324G>A , LRG_2t1:c.1324G>A | NP_000080.2:p.Gly442Arg |
| ENST00000297268.10:c.1324G>A | ENSP00000297268.6:p.Gly442Arg |
| ENST00000620463.1:c.1318G>A | ENSP00000477719.1:p.Gly440Arg |