Linked Data
dbSNP Id:
rs1320195477
gnomAD v2:
9-100614218-C-CCAG
gnomAD v3:
9-97851936-C-CCAG
gnomAD v4:
9-97851936-C-CCAG
MyVariant Identifiers:
chr9:g.100614218_100614219insCAG (hg19)
chr9:g.97851936_97851937insCAG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.97851937_97851938insAGC , CM000671.2:g.97851937_97851938insAGC | GRCh38 |
| NC_000009.11:g.100614219_100614220insAGC , CM000671.1:g.100614219_100614220insAGC | GRCh37 |
| NC_000009.10:g.99654040_99654041insAGC | NCBI36 |
| NG_011979.1:g.3683_3684insAGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_930158.1:n.218+939_218+940insCTG | ||
| XR_930159.1:n.218+939_218+940insCTG | ||
| XR_930160.1:n.218+939_218+940insCTG | ||
| XR_930161.1:n.218+939_218+940insCTG | ||
| NR_147055.1:n.165+979_165+980insCTG |