Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48488411A= , CM000677.2:g.48488411A= | GRCh38 |
| NC_000015.9:g.48780608A= , CM000677.1:g.48780608A= | GRCh37 |
| NC_000015.8:g.46567900A= | NCBI36 |
| NG_008805.2:g.162378T= , LRG_778:g.162378T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000138.5:c.3165T= MANE Select | NP_000129.3:p.Cys1055= |
| ENST00000316623.10:c.3165T= MANE Select | ENSP00000325527.5:p.Cys1055= |
| NM_000138.4:c.3165T= , LRG_778t1:c.3165T= | NP_000129.3:p.Cys1055= |
| ENST00000316623.9:c.3165T= | ENSP00000325527.5:p.Cys1055= |
| ENST00000537463.6:c.637-13761T= | ENSP00000440294.2:n.637-13761T= |
| ENST00000559133.6:c.3165T= | ENSP00000453958.2:p.Cys1055= |
| ENST00000674301.2:c.3165T= | ENSP00000501333.2:p.Cys1055= |
| ENST00000684448.1:n.1839T= |