Linked Data
dbSNP Id:
rs2150384303
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33092684C>G , CM000668.2:g.33092684C>G | GRCh38 |
| NC_000006.11:g.33060461C>G , CM000668.1:g.33060461C>G | GRCh37 |
| NC_000006.10:g.33168439C>G | NCBI36 |
| NG_033242.1:g.21759C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000433582.1:n.300+209G>C |