Linked Data
dbSNP Id:
rs2109066112
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.26083872C>T , CM000666.2:g.26083872C>T | GRCh38 |
| NC_000004.11:g.26085494C>T , CM000666.1:g.26085494C>T | GRCh37 |
| NC_000004.10:g.25694592C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925506.1:n.1401+3282C>T | ||
| XR_925506.3:n.1408+3282C>T |