Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45986949G>A , CM000683.2:g.45986949G>A | GRCh38 |
| NC_000021.8:g.47406863G>A , CM000683.1:g.47406863G>A | GRCh37 |
| NC_000021.7:g.46231291G>A | NCBI36 |
| NG_008674.1:g.10201G>A , LRG_475:g.10201G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001848.3:c.594G>A MANE Select | NP_001839.2:p.Pro198= |
| ENST00000361866.8:c.594G>A MANE Select | ENSP00000355180.3:p.Pro198= |
| NM_001848.2:c.594G>A , LRG_475t1:c.594G>A | NP_001839.2:p.Pro198= |
| ENST00000361866.7:c.594G>A | ENSP00000355180.3:p.Pro198= |
| ENST00000612273.1:c.594G>A | ENSP00000483630.1:p.Pro198= |