Linked Data
dbSNP Id:
rs1783933289
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.22721134C>T , CM000669.2:g.22721134C>T | GRCh38 |
| NC_000007.13:g.22760753C>T , CM000669.1:g.22760753C>T | GRCh37 |
| NC_000007.12:g.22727278C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650428.1:n.46+6434G>A |