Linked Data
dbSNP Id:
rs2128682835
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41772348T>A , CM000669.2:g.41772348T>A | GRCh38 |
| NC_000007.13:g.41811946T>A , CM000669.1:g.41811946T>A | GRCh37 |
| NC_000007.12:g.41778471T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_027118.1:n.359-548T>A | ||
| NR_027118.2:n.356-548T>A | ||
| XR_001745185.1:n.964+36634T>A | ||
| XR_001745186.1:n.954+36644T>A |