Linked Data
gnomAD v4:
16-31096095-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.31096095C>T , CM000678.2:g.31096095C>T | GRCh38 |
| NC_000016.9:g.31107416C>T , CM000678.1:g.31107416C>T | GRCh37 |
| NC_000016.8:g.31014917C>T | NCBI36 |
| NG_011564.1:g.3861G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_950848.1:n.16+227G>A |