Linked Data
gnomAD v4:
11-118304570-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118304570C>T , CM000673.2:g.118304570C>T | GRCh38 |
| NC_000011.9:g.118175285C>T , CM000673.1:g.118175285C>T | GRCh37 |
| NC_000011.8:g.117680495C>T | NCBI36 |
| NG_007383.1:g.4991C>T , LRG_38:g.4991C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.8:c.-266C>T | ENSP00000354566.4:n.-266C>T |