Linked Data
gnomAD v4:
4-52038421-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52038421C>T , CM000666.2:g.52038421C>T | GRCh38 |
| NC_000004.11:g.52904587C>T , CM000666.1:g.52904587C>T | GRCh37 |
| NC_000004.10:g.52599344C>T | NCBI36 |
| NG_008891.1:g.4899G>A , LRG_204:g.4899G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.9:c.-162G>A | ENSP00000370839.5:n.-162G>A |