Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68444825C= , CM000663.2:g.68444825C= | GRCh38 |
| NC_000001.10:g.68910508C= , CM000663.1:g.68910508C= | GRCh37 |
| NC_000001.9:g.68683096C= | NCBI36 |
| NG_008472.1:g.10135G= | |
| NG_008472.2:g.10135G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000329.3:c.304G= MANE Select | NP_000320.1:p.Glu102= |
| ENST00000262340.6:c.304G= MANE Select | ENSP00000262340.5:p.Glu102= |
| NM_000329.2:c.304G= | NP_000320.1:p.Glu102= |
| ENST00000262340.5:c.304G= | ENSP00000262340.5:p.Glu102= |
| XM_017002027.1:c.28G= | XP_016857516.1:p.Glu10= |