Linked Data
dbSNP Id:
rs952851487
gnomAD v3:
9-97851951-C-CCCCA
gnomAD v4:
9-97851951-C-CCCCA
MyVariant Identifiers:
chr9:g.100614233_100614234insCCCA (hg19)
chr9:g.97851951_97851952insCCCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97851951_97851952insCCCA , CM000671.2:g.97851951_97851952insCCCA | GRCh38 |
| NC_000009.11:g.100614233_100614234insCCCA , CM000671.1:g.100614233_100614234insCCCA | GRCh37 |
| NC_000009.10:g.99654054_99654055insCCCA | NCBI36 |
| NG_011979.1:g.3697_3698insCCCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930158.1:n.218+924_218+925insTGGG | ||
| XR_930159.1:n.218+924_218+925insTGGG | ||
| XR_930160.1:n.218+924_218+925insTGGG | ||
| XR_930161.1:n.218+924_218+925insTGGG | ||
| NR_147055.1:n.165+964_165+965insTGGG |