Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177344C= , CM000678.2:g.177344C= | GRCh38 |
| NC_000016.9:g.227343C= , CM000678.1:g.227343C= | GRCh37 |
| NC_000016.8:g.167343C= | NCBI36 |
| NG_000006.1:g.38207C= | |
| NG_059186.1:g.5694C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.362C= MANE Select | NP_000549.1:p.Ala121= |
| ENST00000320868.9:c.362C= MANE Select | ENSP00000322421.5:p.Ala121= |
| NM_000558.4:c.362C= | NP_000549.1:p.Ala121= |
| ENST00000397797.1:c.266C= | ENSP00000380899.1:p.Ala89= |
| ENST00000472694.1:n.498C= |