Linked Data
dbSNP Id:
rs1022986711
gnomAD v3:
17-69854850-C-T
gnomAD v4:
17-69854850-C-T
MyVariant Identifiers:
chr17:g.69854850C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.69854850C>T , CM000679.2:g.69854850C>T | GRCh38 |
| NC_000017.10:g.67850991C>T , CM000679.1:g.67850991C>T | GRCh37 |
| NC_000017.9:g.65362586C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109971.1:n.363+9364C>T | ||
| NR_109972.1:n.363+9364C>T |