Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176956G= , CM000678.2:g.176956G= | GRCh38 |
| NC_000016.9:g.226955G= , CM000678.1:g.226955G= | GRCh37 |
| NC_000016.8:g.166955G= | NCBI36 |
| NG_000006.1:g.37819G= | |
| NG_059186.1:g.5306G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.123G= MANE Select | NP_000549.1:p.Lys41= |
| ENST00000320868.9:c.123G= MANE Select | ENSP00000322421.5:p.Lys41= |
| NM_000558.4:c.123G= | NP_000549.1:p.Lys41= |
| ENST00000397797.1:c.27G= | ENSP00000380899.1:p.Lys9= |
| ENST00000472694.1:n.259G= | |
| ENST00000487791.1:n.92G= |