Linked Data
gnomAD v4:
22-20887957-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20887958dup , CM000684.2:g.20887958dup | GRCh38 |
| NC_000022.10:g.21242246dup , CM000684.1:g.21242246dup | GRCh37 |
| NC_000022.9:g.19572246dup | NCBI36 |
| NG_012152.1:g.33955dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215730.12:c.*122dup MANE Select | ENSP00000215730.6:n.*122dup | |
| ENST00000215730.11:c.*122dup | ENSP00000215730.6:n.*122dup | |
| NM_004782.3:c.*122dup | NP_004773.1:n.*122dup | |
| NM_004782.4:c.*122dup MANE Select | NP_004773.1:n.*122dup |