Linked Data
dbSNP Id:
rs139926691
MyVariant Identifiers:
chr9:g.20145627_20145628insCACA (hg19)
chr9:g.20145629_20145630insCACA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.20145631_20145632insCACA , CM000671.2:g.20145631_20145632insCACA | GRCh38 |
| NC_000009.11:g.20145629_20145630insCACA , CM000671.1:g.20145629_20145630insCACA | GRCh37 |
| NC_000009.10:g.20135629_20135630insCACA | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017014592.1:c.-528-141243_-528-141242insTGTG | XP_016870081.1:n.-528-141243_-528-141242insTGTG |