Linked Data
gnomAD v4:
12-21174773-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174777del , CM000674.2:g.21174777del | GRCh38 |
| NC_000012.11:g.21327711del , CM000674.1:g.21327711del | GRCh37 |
| NC_000012.10:g.21218978del | NCBI36 |
| NG_011745.1:g.48584del , LRG_1022:g.48584del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.359+68del MANE Select | ENSP00000256958.2:n.359+68del | |
| ENST00000256958.2:c.359+68del | ENSP00000256958.2:n.359+68del | |
| ENST00000543498.5:c.426-1999del | ||
| NM_006446.4:c.359+68del , LRG_1022t1:c.359+68del | NP_006437.3:n.359+68del | |
| NM_006446.5:c.359+68del MANE Select | NP_006437.3:n.359+68del |