Linked Data
gnomAD v4:
12-21176778-AC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21176779del , CM000674.2:g.21176779del | GRCh38 |
| NC_000012.11:g.21329713del , CM000674.1:g.21329713del | GRCh37 |
| NC_000012.10:g.21220980del | NCBI36 |
| NG_011745.1:g.50586del , LRG_1022:g.50586del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000256958.3:c.363del MANE Select | ENSP00000256958.2:p.Tyr121Ter | |
| ENST00000256958.2:c.363del | ENSP00000256958.2:p.Tyr121Ter | |
| ENST00000543498.5:c.429del | ||
| NM_006446.4:c.363del , LRG_1022t1:c.363del | NP_006437.3:p.Tyr121Ter | |
| NM_006446.5:c.363del MANE Select | NP_006437.3:p.Tyr121Ter |