Linked Data
gnomAD v4:
20-53566935-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.53566935T>C , CM000682.2:g.53566935T>C | GRCh38 |
| NC_000020.10:g.52183474T>C , CM000682.1:g.52183474T>C | GRCh37 |
| NC_000020.9:g.51616881T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110051.1:n.556-3337T>C |