Linked Data
gnomAD v4:
11-6319060-G-GT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6319061dup , CM000673.2:g.6319061dup | GRCh38 |
| NC_000011.9:g.6340291dup , CM000673.1:g.6340291dup | GRCh37 |
| NC_000011.8:g.6296867dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303927.4:c.*102dup MANE Select | ENSP00000307292.3:n.*102dup | |
| ENST00000303927.3:c.*102dup | ENSP00000307292.3:n.*102dup | |
| ENST00000532354.1:n.910dup | ||
| NM_145040.2:c.*102dup | NP_659477.2:n.*102dup | |
| XR_930997.1:n.720+841dup | ||
| NM_145040.3:c.*102dup MANE Select | NP_659477.2:n.*102dup |