Linked Data
dbSNP Id:
rs1454780286
gnomAD v3:
17-36088101-G-A
gnomAD v4:
17-36088101-G-A
MyVariant Identifiers:
chr17:g.36088101G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088101G>A , CM000679.2:g.36088101G>A | GRCh38 |
| NC_000017.10:g.34415447G>A , CM000679.1:g.34415447G>A | GRCh37 |
| NC_000017.9:g.31439560G>A | NCBI36 |
| NG_027730.1:g.7060C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001752857.1:n.1637-1445G>A | ||
| XR_001752858.1:n.673-1445G>A | ||
| XR_001752859.1:n.1584-1445G>A |