Linked Data
dbSNP Id:
rs1022497572
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.69854511G>C , CM000679.2:g.69854511G>C | GRCh38 |
| NC_000017.10:g.67850652G>C , CM000679.1:g.67850652G>C | GRCh37 |
| NC_000017.9:g.65362247G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109971.1:n.363+9025G>C | ||
| NR_109972.1:n.363+9025G>C |