Linked Data
gnomAD v4:
1-45329235-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45329235C>T , CM000663.2:g.45329235C>T | GRCh38 |
| NC_000001.10:g.45794907C>T , CM000663.1:g.45794907C>T | GRCh37 |
| NC_000001.9:g.45567494C>T | NCBI36 |
| NG_008189.1:g.16236G>A , LRG_220:g.16236G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529984.5:c.*71G>A | ENSP00000437093.1:n.*71G>A |