Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177319C= , CM000678.2:g.177319C= | GRCh38 |
| NC_000016.9:g.227318C= , CM000678.1:g.227318C= | GRCh37 |
| NC_000016.8:g.167318C= | NCBI36 |
| NG_000006.1:g.38182C= | |
| NG_059186.1:g.5669C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.337C= MANE Select | NP_000549.1:p.His113= |
| ENST00000320868.9:c.337C= MANE Select | ENSP00000322421.5:p.His113= |
| NM_000558.4:c.337C= | NP_000549.1:p.His113= |
| ENST00000397797.1:c.241C= | ENSP00000380899.1:p.His81= |
| ENST00000472694.1:n.473C= |