Linked Data
dbSNP Id:
rs1763385038
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33092690T>G , CM000668.2:g.33092690T>G | GRCh38 |
| NC_000006.11:g.33060467T>G , CM000668.1:g.33060467T>G | GRCh37 |
| NC_000006.10:g.33168445T>G | NCBI36 |
| NG_033242.1:g.21765T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000433582.1:n.300+203A>C |