Linked Data
dbSNP Id:
rs766120201
gnomAD v2:
5-44662549-A-ATTTC
gnomAD v3:
5-44662447-A-ATTTC
gnomAD v4:
5-44662447-A-ATTTC
MyVariant Identifiers:
chr5:g.44662549_44662550insTTTC (hg19)
chr5:g.44662447_44662448insTTTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.44662451_44662454dup , CM000667.2:g.44662451_44662454dup | GRCh38 |
| NC_000005.9:g.44662553_44662556dup , CM000667.1:g.44662553_44662556dup | GRCh37 |
| NC_000005.8:g.44698310_44698313dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_427699.2:n.92-3894_92-3891dup | ||
| XR_925983.1:n.71-3894_71-3891dup |