Canonical Allele Identifier:
CA784578979
Gene:
Linked Data
dbSNP Id:
rs911541189
gnomAD v3:
4-102499665-A-ACCTC
gnomAD v4:
4-102499665-A-ACCTC
MyVariant Identifiers:
chr4:g.103420822_103420823insCCTC (hg19)
chr4:g.102499665_102499666insCCTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499682_102499685dup , CM000666.2:g.102499682_102499685dup | GRCh38 |
| NC_000004.11:g.103420839_103420842dup , CM000666.1:g.103420839_103420842dup | GRCh37 |
| NC_000004.10:g.103639871_103639874dup | NCBI36 |
| NG_050628.1:g.3354_3357dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1580_643+1583dup | XP_011530769.1:n.643+1580_643+1583dup | |
| NR_136202.1:n.48+2770_48+2773dup |