Linked Data
dbSNP Id:
rs1763381631
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33092577C>T , CM000668.2:g.33092577C>T | GRCh38 |
| NC_000006.11:g.33060354C>T , CM000668.1:g.33060354C>T | GRCh37 |
| NC_000006.10:g.33168332C>T | NCBI36 |
| NG_033242.1:g.21652C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000433582.1:n.301-177G>A |