Linked Data
gnomAD v4:
20-53566956-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.53566956C>T , CM000682.2:g.53566956C>T | GRCh38 |
| NC_000020.10:g.52183495C>T , CM000682.1:g.52183495C>T | GRCh37 |
| NC_000020.9:g.51616902C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110051.1:n.556-3316C>T |