Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.165419877T= , CM000663.2:g.165419877T= | GRCh38 |
| NC_000001.10:g.165389114T= , CM000663.1:g.165389114T= | GRCh37 |
| NC_000001.9:g.163655738T= | NCBI36 |
| NG_029517.1:g.30479A= | |
| NG_029517.2:g.30479A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359842.10:c.435A= MANE Select | ENSP00000352900.5:p.Arg145= | |
| ENST00000359842.9:c.435A= | ENSP00000352900.5:p.Arg145= | |
| ENST00000470566.1:n.360A= | ||
| ENST00000619224.1:c.66A= | ENSP00000482458.1:p.Arg22= | |
| NM_001256570.1:c.66A= | NP_001243499.1:p.Arg22= | |
| NM_001256571.1:c.66A= | NP_001243500.1:p.Arg22= | |
| NM_006917.4:c.435A= | NP_008848.1:p.Arg145= | |
| NM_006917.5:c.435A= MANE Select | NP_008848.1:p.Arg145= | |
| NM_001256571.2:c.66A= | NP_001243500.1:p.Arg22= | |
| NM_001256570.2:c.66A= | NP_001243499.1:p.Arg22= |