Linked Data
gnomAD v4:
11-2171839-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2171841del , CM000673.2:g.2171841del | GRCh38 |
| NC_000011.9:g.2193071del , CM000673.1:g.2193071del | GRCh37 |
| NC_000011.8:g.2149647del | NCBI36 |
| NG_008128.1:g.4966del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352909.7:c.-54del | ENSP00000325951.3:n.-54del | |
| XM_011520335.1:c.-54del | XP_011518637.1:n.-54del | |
| XM_011520335.2:c.-54del | XP_011518637.1:n.-54del |