Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431160A= , CM000663.2:g.68431160A= | GRCh38 |
| NC_000001.10:g.68896843A= , CM000663.1:g.68896843A= | GRCh37 |
| NC_000001.9:g.68669431A= | NCBI36 |
| NG_008472.1:g.23800T= | |
| NG_008472.2:g.23800T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000329.3:c.1355T= MANE Select | NP_000320.1:p.Val452= |
| ENST00000262340.6:c.1355T= MANE Select | ENSP00000262340.5:p.Val452= |
| NM_000329.2:c.1355T= | NP_000320.1:p.Val452= |
| ENST00000262340.5:c.1355T= | ENSP00000262340.5:p.Val452= |
| XM_017002027.1:c.1079T= | XP_016857516.1:p.Val360= |