Linked Data
dbSNP Id:
rs766779361
ExAC:
6:32008013 TC / T
gnomAD v3:
6-32040236-TC-T
gnomAD v4:
6-32040236-TC-T
MyVariant Identifiers:
chr6:g.32008014del (hg19)
chr6:g.32040238del (hg38)
chr6:g.32040237del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32040239del , CM000668.2:g.32040239del | GRCh38 |
| NC_000006.11:g.32008016del , CM000668.1:g.32008016del | GRCh37 |
| NC_000006.10:g.32115995del | NCBI36 |
| NG_007941.2:g.6932del | |
| NG_008337.2:g.74138del | |
| NG_007941.3:g.6935del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644719.2:c.939+34del MANE Select | ENSP00000496625.1:n.939+34del | |
| ENST00000418967.6:c.939+34del | ENSP00000408860.2:n.939+34del | |
| ENST00000435122.3:c.849+34del | ENSP00000415043.2:n.849+34del | |
| ENST00000479074.5:n.997+34del | ||
| ENST00000479730.5:n.1055+34del | ||
| ENST00000483041.5:n.1108+34del | ||
| ENST00000486063.5:n.919-167del | ||
| NM_000500.7:c.939+34del | NP_000491.4:n.939+34del | |
| NM_001128590.3:c.849+34del | NP_001122062.3:n.849+34del | |
| XM_011514314.1:c.534+34del | XP_011512616.1:n.534+34del | |
| NM_000500.9:c.939+34del MANE Select | NP_000491.4:n.939+34del | |
| NM_001368143.1:c.534+34del | NP_001355072.1:n.534+34del | |
| NM_001368144.1:c.534+34del | NP_001355073.1:n.534+34del | |
| NM_001128590.4:c.849+34del | NP_001122062.3:n.849+34del | |
| NM_001368143.2:c.534+34del | NP_001355072.1:n.534+34del | |
| NM_001368144.2:c.534+34del | NP_001355073.1:n.534+34del |