Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.52236941T= , CM000668.2:g.52236941T= | GRCh38 |
| NC_000006.11:g.52101739T= , CM000668.1:g.52101739T= | GRCh37 |
| NC_000006.10:g.52209698T= | NCBI36 |
| NG_031869.1:g.12560A= , LRG_356:g.12560A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_052872.4:c.482A= MANE Select | NP_443104.1:p.His161= |
| ENST00000336123.5:c.482A= MANE Select | ENSP00000337432.4:p.His161= |
| NM_052872.3:c.482A= , LRG_356t1:c.482A= | NP_443104.1:p.His161= |
| ENST00000336123.4:c.482A= | ENSP00000337432.4:p.His161= |
| ENST00000478427.1:n.666A= | |
| ENST00000699946.1:c.482A= | ENSP00000514702.1:p.His161= |
| XM_011514276.1:c.482A= | XP_011512578.1:p.His161= |