Linked Data
gnomAD v4:
11-6319079-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319081dup , CM000673.2:g.6319081dup | GRCh38 |
| NC_000011.9:g.6340311dup , CM000673.1:g.6340311dup | GRCh37 |
| NC_000011.8:g.6296887dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*83dup MANE Select | ENSP00000307292.3:n.*83dup | |
| ENST00000303927.3:c.*83dup | ENSP00000307292.3:n.*83dup | |
| ENST00000532354.1:n.891dup | ||
| NM_145040.2:c.*83dup | NP_659477.2:n.*83dup | |
| XR_930997.1:n.720+861dup | ||
| NM_145040.3:c.*83dup MANE Select | NP_659477.2:n.*83dup |