Linked Data
gnomAD v4:
11-2171886-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2171886C>T , CM000673.2:g.2171886C>T | GRCh38 |
| NC_000011.9:g.2193116C>T , CM000673.1:g.2193116C>T | GRCh37 |
| NC_000011.8:g.2149692C>T | NCBI36 |
| NG_008128.1:g.4920G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011520335.1:c.-100G>A | XP_011518637.1:n.-100G>A | |
| XM_011520335.2:c.-100G>A | XP_011518637.1:n.-100G>A |