Linked Data
dbSNP Id:
rs1207574045
gnomAD v2:
9-20145789-G-GTGTATATGC
gnomAD v3:
9-20145791-G-GTGTATATGC
gnomAD v4:
9-20145791-G-GTGTATATGC
MyVariant Identifiers:
chr9:g.20145789_20145790insTGTATATGC (hg19)
chr9:g.20145791_20145792insTGTATATGC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.20145792_20145800dup , CM000671.2:g.20145792_20145800dup | GRCh38 |
| NC_000009.11:g.20145790_20145798dup , CM000671.1:g.20145790_20145798dup | GRCh37 |
| NC_000009.10:g.20135790_20135798dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017014592.1:c.-528-141413_-528-141405dup | XP_016870081.1:n.-528-141413_-528-141405dup |