Linked Data
MyVariant Identifiers:
chr3:g.180377336A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659548A>C , CM000665.2:g.180659548A>C | GRCh38 |
| NC_000003.11:g.180377336A>C , CM000665.1:g.180377336A>C | GRCh37 |
| NC_000003.10:g.181860030A>C | NCBI36 |
| NG_029581.1:g.24948T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.642T>G MANE Select | ENSP00000417960.2:p.Arg214= | |
| ENST00000650641.1:n.721T>G | ||
| ENST00000650889.1:n.814T>G | ||
| ENST00000651046.1:c.642T>G | ENSP00000499175.1:p.Arg214= | |
| ENST00000651818.1:n.784T>G | ||
| ENST00000652024.1:n.733T>G | ||
| ENST00000652408.1:n.779T>G | ||
| ENST00000442201.6:c.642T>G | ENSP00000405708.2:p.Arg214= | |
| ENST00000476379.5:c.642T>G | ENSP00000417960.1:p.Arg214= | |
| NM_181426.1:c.642T>G | NP_852091.1:p.Arg214= | |
| NM_181426.2:c.642T>G MANE Select | NP_852091.1:p.Arg214= |