Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31541293A>G , CM000680.2:g.31541293A>G | GRCh38 |
| NC_000018.9:g.29121256A>G , CM000680.1:g.29121256A>G | GRCh37 |
| NC_000018.8:g.27375254A>G | NCBI36 |
| NG_007072.3:g.48052A>G , LRG_397:g.48052A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.1980A>G MANE Select | ENSP00000261590.8:p.Glu660= | |
| ENST00000261590.12:c.1980A>G | ENSP00000261590.8:p.Glu660= | |
| NM_001943.3:c.1980A>G , LRG_397t1:c.1980A>G | NP_001934.2:p.Glu660= | |
| NM_001943.4:c.1980A>G | NP_001934.2:p.Glu660= | |
| XM_024451095.1:c.1446A>G | XP_024306863.1:p.Glu482= | |
| NM_001943.5:c.1980A>G MANE Select | NP_001934.2:p.Glu660= |