Linked Data
dbSNP Id:
rs1583641782
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41772345T>C , CM000669.2:g.41772345T>C | GRCh38 |
| NC_000007.13:g.41811943T>C , CM000669.1:g.41811943T>C | GRCh37 |
| NC_000007.12:g.41778468T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_027118.1:n.359-551T>C | ||
| NR_027118.2:n.356-551T>C | ||
| XR_001745185.1:n.964+36631T>C | ||
| XR_001745186.1:n.954+36641T>C |