Linked Data
gnomAD v4:
1-119140817-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119140820dup , CM000663.2:g.119140820dup | GRCh38 |
| NC_000001.10:g.119683443dup , CM000663.1:g.119683443dup | GRCh37 |
| NC_000001.9:g.119484966dup | NCBI36 |
| NG_050658.1:g.4971dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125974.1:n.398+27dup | ||
| NR_125975.1:n.398+27dup | ||
| NR_125976.1:n.398+27dup | ||
| NR_125977.1:n.398+27dup |