Linked Data
dbSNP Id:
rs7067478
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.7779316A>C , CM000686.2:g.7779316A>C | GRCh38 |
| NC_000024.9:g.7647357A>C , CM000686.1:g.7647357A>C | GRCh37 |
| NC_000024.8:g.7707357A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651261.1:n.115-2612T>G | ||
| ENST00000652723.1:n.1027-2612T>G | ||
| ENST00000442584.2:n.219-2288T>G |