Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659705T= , CM000665.2:g.180659705T= | GRCh38 |
| NC_000003.11:g.180377493T= , CM000665.1:g.180377493T= | GRCh37 |
| NC_000003.10:g.181860187T= | NCBI36 |
| NG_029581.1:g.24791A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.581A= MANE Select | ENSP00000417960.2:p.Asn194= | |
| ENST00000650641.1:n.660A= | ||
| ENST00000650889.1:n.753A= | ||
| ENST00000651046.1:c.581A= | ENSP00000499175.1:p.Asn194= | |
| ENST00000651818.1:n.723A= | ||
| ENST00000652024.1:n.672A= | ||
| ENST00000652408.1:n.718A= | ||
| ENST00000442201.6:c.581A= | ENSP00000405708.2:p.Asn194= | |
| ENST00000476379.5:c.581A= | ENSP00000417960.1:p.Asn194= | |
| NM_181426.1:c.581A= | NP_852091.1:p.Asn194= | |
| NM_181426.2:c.581A= MANE Select | NP_852091.1:p.Asn194= |