Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985896C= , CM000678.2:g.1985896C= | GRCh38 |
| NC_000016.9:g.2035897C= , CM000678.1:g.2035897C= | GRCh37 |
| NC_000016.8:g.1975898C= | NCBI36 |
| NG_016288.1:g.6748C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000567719.2:c.261C= | ENSP00000455885.1:p.Thr87= | |
| ENST00000248114.7:c.486C= MANE Select | ENSP00000248114.6:p.Thr162= | |
| ENST00000248114.6:c.486C= | ENSP00000248114.6:p.Thr162= | |
| ENST00000565658.1:n.643C= | ||
| ENST00000567719.1:c.261C= | ENSP00000455885.1:p.Thr87= | |
| ENST00000569451.1:c.289C= | ENSP00000456432.1:p.Pro97= | |
| NM_005262.2:c.486C= | NP_005253.3:p.Thr162= | |
| NM_005262.3:c.486C= MANE Select | NP_005253.3:p.Thr162= |