Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154158G>A , CM000681.2:g.55154158G>A | GRCh38 |
| NC_000019.9:g.55665526G>A , CM000681.1:g.55665526G>A | GRCh37 |
| NC_000019.8:g.60357338G>A | NCBI36 |
| NG_007866.2:g.8575C>T , LRG_432:g.8575C>T | |
| NG_011829.2:g.81C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000363.5:c.421C>T MANE Select | NP_000354.4:p.Arg141Trp |
| ENST00000344887.10:c.421C>T MANE Select | ENSP00000341838.5:p.Arg141Trp |
| NM_000363.4:c.421C>T , LRG_432t1:c.421C>T | NP_000354.4:p.Arg141Trp |
| ENST00000344887.9:c.421C>T | ENSP00000341838.5:p.Arg141Trp |
| ENST00000585806.5:n.420C>T | |
| ENST00000586669.5:n.429C>T | |
| ENST00000588882.1:c.346C>T | ENSP00000466729.1:p.Arg116Trp |
| ENST00000589864.1:n.249C>T | |
| ENST00000665070.1:c.454C>T | ENSP00000499482.1:p.Arg152Trp |