Linked Data
dbSNP Id:
rs1188190095
gnomAD v4:
17-36088208-A-G
MyVariant Identifiers:
chr17:g.36088208A>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088208A>G , CM000679.2:g.36088208A>G | GRCh38 |
| NC_000017.10:g.34415554A>G , CM000679.1:g.34415554A>G | GRCh37 |
| NC_000017.9:g.31439667A>G | NCBI36 |
| NG_027730.1:g.6953T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001752857.1:n.1637-1338A>G | ||
| XR_001752858.1:n.673-1338A>G | ||
| XR_001752859.1:n.1584-1338A>G |