Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659538T>A , CM000665.2:g.180659538T>A | GRCh38 |
| NC_000003.11:g.180377326T>A , CM000665.1:g.180377326T>A | GRCh37 |
| NC_000003.10:g.181860020T>A | NCBI36 |
| NG_029581.1:g.24958A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.652A>T MANE Select | ENSP00000417960.2:p.Asn218Tyr | |
| ENST00000650641.1:n.731A>T | ||
| ENST00000650889.1:n.824A>T | ||
| ENST00000651046.1:c.652A>T | ENSP00000499175.1:p.Asn218Tyr | |
| ENST00000651818.1:n.794A>T | ||
| ENST00000652024.1:n.743A>T | ||
| ENST00000652408.1:n.789A>T | ||
| ENST00000442201.6:c.652A>T | ENSP00000405708.2:p.Asn218Tyr | |
| ENST00000476379.5:c.652A>T | ENSP00000417960.1:p.Asn218Tyr | |
| NM_181426.1:c.652A>T | NP_852091.1:p.Asn218Tyr | |
| NM_181426.2:c.652A>T MANE Select | NP_852091.1:p.Asn218Tyr |