Linked Data
gnomAD v4:
3-180659676-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659676C>G , CM000665.2:g.180659676C>G | GRCh38 |
| NC_000003.11:g.180377464C>G , CM000665.1:g.180377464C>G | GRCh37 |
| NC_000003.10:g.181860158C>G | NCBI36 |
| NG_029581.1:g.24820G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.609+1G>C MANE Select | ENSP00000417960.2:n.609+1G>C | |
| ENST00000650641.1:n.688+1G>C | ||
| ENST00000650889.1:n.781+1G>C | ||
| ENST00000651046.1:c.609+1G>C | ENSP00000499175.1:n.609+1G>C | |
| ENST00000651818.1:n.751+1G>C | ||
| ENST00000652024.1:n.700+1G>C | ||
| ENST00000652408.1:n.746+1G>C | ||
| ENST00000442201.6:c.609+1G>C | ENSP00000405708.2:n.609+1G>C | |
| ENST00000476379.5:c.609+1G>C | ENSP00000417960.1:n.609+1G>C | |
| NM_181426.1:c.609+1G>C | NP_852091.1:n.609+1G>C | |
| NM_181426.2:c.609+1G>C MANE Select | NP_852091.1:n.609+1G>C |