Linked Data
gnomAD v4:
17-4734425-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4734425G>A , CM000679.2:g.4734425G>A | GRCh38 |
| NC_000017.10:g.4637720G>A , CM000679.1:g.4637720G>A | GRCh37 |
| NC_000017.9:g.4584469G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293778.12:c.*78C>T MANE Select | ENSP00000293778.7:n.*78C>T | |
| ENST00000574412.6:c.*181C>T | ENSP00000459592.2:n.*181C>T | |
| ENST00000293778.10:c.*78C>T | ENSP00000293778.6:n.*78C>T | |
| ENST00000574412.5:c.*181C>T | ENSP00000459592.1:n.*181C>T | |
| ENST00000576153.5:n.634C>T | ||
| NM_022059.3:c.*78C>T | NP_071342.2:n.*78C>T | |
| NM_022059.4:c.*78C>T | NP_071342.2:n.*78C>T | |
| NM_001386809.1:c.*78C>T MANE Select | NP_001373738.1:n.*78C>T |