Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45992028G>A , CM000683.2:g.45992028G>A | GRCh38 |
| NC_000021.8:g.47411942G>A , CM000683.1:g.47411942G>A | GRCh37 |
| NC_000021.7:g.46236370G>A | NCBI36 |
| NG_008674.1:g.15280G>A , LRG_475:g.15280G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.1138G>A MANE Select | NP_001839.2:p.Gly380Arg |
| ENST00000361866.8:c.1138G>A MANE Select | ENSP00000355180.3:p.Gly380Arg |
| NM_001848.2:c.1138G>A , LRG_475t1:c.1138G>A | NP_001839.2:p.Gly380Arg |
| ENST00000361866.7:c.1138G>A | ENSP00000355180.3:p.Gly380Arg |
| ENST00000612273.1:c.1138G>A | ENSP00000483630.1:p.Gly380Arg |