Linked Data
gnomAD v4:
1-229431145-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229431145C>T , CM000663.2:g.229431145C>T | GRCh38 |
| NC_000001.10:g.229566892C>T , CM000663.1:g.229566892C>T | GRCh37 |
| NC_000001.9:g.227633515C>T | NCBI36 |
| NG_006672.1:g.7952G>A , LRG_429:g.7952G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684723.1:c.*354G>A | ENSP00000508084.1:n.*354G>A |