Linked Data
gnomAD v4:
6-32220809-G-GT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32220810dup , CM000668.2:g.32220810dup | GRCh38 |
| NC_000006.11:g.32188587dup , CM000668.1:g.32188587dup | GRCh37 |
| NC_000006.10:g.32296565dup | NCBI36 |
| NG_028190.1:g.8258dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.868dup MANE Select | ENSP00000364163.3:p.Thr290AsnfsTer28 | |
| ENST00000473562.1:n.997dup | ||
| NM_004557.3:c.868dup | NP_004548.3:p.Thr290AsnfsTer28 | |
| NR_134949.1:n.1007dup | ||
| NR_134950.1:n.1007dup | ||
| NM_004557.4:c.868dup MANE Select | NP_004548.3:p.Thr290AsnfsTer28 | |
| NR_134949.2:n.1007dup | ||
| NR_134950.2:n.1007dup |