Linked Data
dbSNP Id:
rs1182421657
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.46108578T>C , CM000684.2:g.46108578T>C | GRCh38 |
| NC_000022.10:g.46504458T>C , CM000684.1:g.46504458T>C | GRCh37 |
| NC_000022.9:g.44883122T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_027033.2:n.373-689T>C | ||
| NR_110479.1:n.315-689T>C |