Linked Data
gnomAD v4:
4-52038363-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52038363C>T , CM000666.2:g.52038363C>T | GRCh38 |
| NC_000004.11:g.52904529C>T , CM000666.1:g.52904529C>T | GRCh37 |
| NC_000004.10:g.52599286C>T | NCBI36 |
| NG_008891.1:g.4957G>A , LRG_204:g.4957G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.9:c.-104G>A | ENSP00000370839.5:n.-104G>A |