Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.82148514C= , CM000678.2:g.82148514C= | GRCh38 |
| NC_000016.9:g.82182119C= , CM000678.1:g.82182119C= | GRCh37 |
| NC_000016.8:g.80739620C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258169.9:c.*217G= MANE Select | ENSP00000258169.4:n.*217G= | |
| ENST00000258169.8:c.*217G= | ENSP00000258169.4:n.*217G= | |
| ENST00000563100.5:c.*72+145G= | ENSP00000454996.1:n.*72+145G= | |
| NM_005792.2:c.*217G= MANE Select | NP_005783.2:n.*217G= | |
| XM_011522808.1:c.*217G= | XP_011521110.1:n.*217G= | |
| XM_011522808.3:c.*217G= | XP_011521110.1:n.*217G= |