Linked Data
dbSNP Id:
rs988494238
gnomAD v2:
11-102656430-C-CTGGT
gnomAD v3:
11-102785699-C-CTGGT
gnomAD v4:
11-102785699-C-CTGGT
MyVariant Identifiers:
chr11:g.102656430_102656431insTGGT (hg19)
chr11:g.102785699_102785700insTGGT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102785701_102785704dup , CM000673.2:g.102785701_102785704dup | GRCh38 |
| NC_000011.9:g.102656432_102656435dup , CM000673.1:g.102656432_102656435dup | GRCh37 |
| NC_000011.8:g.102161642_102161645dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371455.7:n.325-12323_325-12320dup | ||
| ENST00000525739.6:n.389+1637_389+1640dup | ||
| ENST00000544704.1:n.344+1637_344+1640dup | ||
| NR_038390.1:n.389+1637_389+1640dup |