Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429727G= , CM000663.2:g.68429727G= | GRCh38 |
| NC_000001.10:g.68895410G= , CM000663.1:g.68895410G= | GRCh37 |
| NC_000001.9:g.68667998G= | NCBI36 |
| NG_008472.1:g.25233C= | |
| NG_008472.2:g.25233C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.*49C= MANE Select | ENSP00000262340.5:n.*49C= | |
| ENST00000262340.5:c.*49C= | ENSP00000262340.5:n.*49C= | |
| NM_000329.2:c.*49C= | NP_000320.1:n.*49C= | |
| XM_017002027.1:c.*49C= | XP_016857516.1:n.*49C= | |
| NM_000329.3:c.*49C= MANE Select | NP_000320.1:n.*49C= |