Linked Data
dbSNP Id:
rs66806500
gnomAD v2:
9-100614217-G-GCCCC
gnomAD v3:
9-97851935-G-GCCCC
gnomAD v4:
9-97851935-G-GCCCC
MyVariant Identifiers:
chr9:g.100614217_100614218insCCCC (hg19)
chr9:g.97851935_97851936insCCCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97851938_97851939insCCCC , CM000671.2:g.97851938_97851939insCCCC | GRCh38 |
| NC_000009.11:g.100614220_100614221insCCCC , CM000671.1:g.100614220_100614221insCCCC | GRCh37 |
| NC_000009.10:g.99654041_99654042insCCCC | NCBI36 |
| NG_011979.1:g.3684_3685insCCCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930158.1:n.218+940_218+941insGGGG | ||
| XR_930159.1:n.218+940_218+941insGGGG | ||
| XR_930160.1:n.218+940_218+941insGGGG | ||
| XR_930161.1:n.218+940_218+941insGGGG | ||
| NR_147055.1:n.165+980_165+981insGGGG |