Linked Data
dbSNP Id:
rs1291700408
gnomAD v3:
11-14893676-TCG-T
gnomAD v4:
11-14893676-TCG-T
MyVariant Identifiers:
chr11:g.14893677_14893678del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893678_14893679del , CM000673.2:g.14893678_14893679del | GRCh38 |
| NC_000011.9:g.14915224_14915225del , CM000673.1:g.14915224_14915225del | GRCh37 |
| NC_000011.8:g.14871800_14871801del | NCBI36 |
| NG_007936.1:g.3528_3529del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011519898.1:c.-1434_-1433del | XP_011518200.1:n.-1434_-1433del | |
| XM_011519898.3:c.-1434_-1433del | XP_011518200.1:n.-1434_-1433del |