Linked Data
gnomAD v4:
3-129530736-GCT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.129530742_129530743del , CM000665.2:g.129530742_129530743del | GRCh38 |
| NC_000003.11:g.129249585_129249586del , CM000665.1:g.129249585_129249586del | GRCh37 |
| NC_000003.10:g.130732275_130732276del | NCBI36 |
| NG_009115.1:g.7104_7105del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296271.4:c.362-134_362-133del MANE Select | ENSP00000296271.3:n.362-134_362-133del | |
| ENST00000296271.3:c.362-134_362-133del | ENSP00000296271.3:n.362-134_362-133del | |
| NM_000539.3:c.362-134_362-133del MANE Select | NP_000530.1:n.362-134_362-133del |