Linked Data
dbSNP Id:
rs1270570882
MyVariant Identifiers:
chr9:g.100614232_100614233insCCA (hg19)
chr9:g.97851950_97851951insCCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97851951_97851952insCAC , CM000671.2:g.97851951_97851952insCAC | GRCh38 |
| NC_000009.11:g.100614233_100614234insCAC , CM000671.1:g.100614233_100614234insCAC | GRCh37 |
| NC_000009.10:g.99654054_99654055insCAC | NCBI36 |
| NG_011979.1:g.3697_3698insCAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930158.1:n.218+925_218+926insTGG | ||
| XR_930159.1:n.218+925_218+926insTGG | ||
| XR_930160.1:n.218+925_218+926insTGG | ||
| XR_930161.1:n.218+925_218+926insTGG | ||
| NR_147055.1:n.165+965_165+966insTGG |