Linked Data
gnomAD v4:
11-5253127-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5253127C>A , CM000673.2:g.5253127C>A | GRCh38 |
| NC_000011.9:g.5274357C>A , CM000673.1:g.5274357C>A | GRCh37 |
| NC_000011.8:g.5230933C>A | NCBI36 |
| NG_000007.3:g.44489G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642908.1:c.315+1165G>T | ENSP00000495346.1:n.315+1165G>T | |
| ENST00000647543.1:c.378+216G>T | ENSP00000496470.1:n.378+216G>T | |
| ENST00000620888.4:c.315+1165G>T | ENSP00000479637.1:n.315+1165G>T |