Linked Data
dbSNP Id:
rs1830592269
gnomAD v3:
9-97851933-C-CCG
gnomAD v4:
9-97851933-C-CCG
MyVariant Identifiers:
chr9:g.100614215_100614216insCG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97851933_97851934insCG , CM000671.2:g.97851933_97851934insCG | GRCh38 |
| NC_000009.11:g.100614215_100614216insCG , CM000671.1:g.100614215_100614216insCG | GRCh37 |
| NC_000009.10:g.99654036_99654037insCG | NCBI36 |
| NG_011979.1:g.3679_3680insCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930158.1:n.218+942_218+943insCG | ||
| XR_930159.1:n.218+942_218+943insCG | ||
| XR_930160.1:n.218+942_218+943insCG | ||
| XR_930161.1:n.218+942_218+943insCG | ||
| NR_147055.1:n.165+982_165+983insCG |