Linked Data
gnomAD v4:
3-180659766-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659766G>T , CM000665.2:g.180659766G>T | GRCh38 |
| NC_000003.11:g.180377554G>T , CM000665.1:g.180377554G>T | GRCh37 |
| NC_000003.10:g.181860248G>T | NCBI36 |
| NG_029581.1:g.24730C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.520C>A MANE Select | ENSP00000417960.2:p.Leu174Met | |
| ENST00000650641.1:n.599C>A | ||
| ENST00000650889.1:n.692C>A | ||
| ENST00000651046.1:c.520C>A | ENSP00000499175.1:p.Leu174Met | |
| ENST00000651818.1:n.662C>A | ||
| ENST00000652024.1:n.611C>A | ||
| ENST00000652408.1:n.657C>A | ||
| ENST00000442201.6:c.520C>A | ENSP00000405708.2:p.Leu174Met | |
| ENST00000476379.5:c.520C>A | ENSP00000417960.1:p.Leu174Met | |
| NM_181426.1:c.520C>A | NP_852091.1:p.Leu174Met | |
| NM_181426.2:c.520C>A MANE Select | NP_852091.1:p.Leu174Met |