Linked Data
gnomAD v4:
14-20892212-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.20892214del , CM000676.2:g.20892214del | GRCh38 |
| NC_000014.8:g.21360373del , CM000676.1:g.21360373del | GRCh37 |
| NC_000014.7:g.20430213del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304639.4:c.*45del MANE Select | ENSP00000302324.3:n.*45del | |
| ENST00000304639.3:c.*45del | ENSP00000302324.3:n.*45del | |
| NM_002935.2:c.*45del | NP_002926.2:n.*45del | |
| XR_110261.2:n.209-16470del | ||
| XR_110261.3:n.726-16470del | ||
| NM_002935.3:c.*45del MANE Select | NP_002926.2:n.*45del |