Linked Data
dbSNP Id:
rs1289874714
gnomAD v3:
17-36088074-T-C
gnomAD v4:
17-36088074-T-C
MyVariant Identifiers:
chr17:g.36088074T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.36088074T>C , CM000679.2:g.36088074T>C | GRCh38 |
| NC_000017.10:g.34415420T>C , CM000679.1:g.34415420T>C | GRCh37 |
| NC_000017.9:g.31439533T>C | NCBI36 |
| NG_027730.1:g.7087A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001752857.1:n.1637-1472T>C | ||
| XR_001752858.1:n.673-1472T>C | ||
| XR_001752859.1:n.1584-1472T>C |