Linked Data
gnomAD v4:
1-45329222-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45329229dup , CM000663.2:g.45329229dup | GRCh38 |
| NC_000001.10:g.45794901dup , CM000663.1:g.45794901dup | GRCh37 |
| NC_000001.9:g.45567488dup | NCBI36 |
| NG_008189.1:g.16248dup , LRG_220:g.16248dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529984.5:c.*83dup | ENSP00000437093.1:n.*83dup |