Linked Data
dbSNP Id:
rs946122525
gnomAD v2:
11-102669122-G-GT
gnomAD v3:
11-102798391-G-GT
gnomAD v4:
11-102798391-G-GT
MyVariant Identifiers:
chr11:g.102669122_102669123insT (hg19)
chr11:g.102798391_102798392insT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798395dup , CM000673.2:g.102798395dup | GRCh38 |
| NC_000011.9:g.102669126dup , CM000673.1:g.102669126dup | GRCh37 |
| NC_000011.8:g.102174336dup | NCBI36 |
| NG_011740.1:g.4844dup | |
| NG_011740.2:g.4844dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371455.7:n.423+273dup | ||
| ENST00000525739.6:n.682+273dup | ||
| ENST00000544704.1:n.443+273dup | ||
| NR_038390.1:n.682+273dup |