Linked Data
dbSNP Id:
rs1009982449
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.108267145C>G , CM000675.2:g.108267145C>G | GRCh38 |
| NC_000013.10:g.108919493C>G , CM000675.1:g.108919493C>G | GRCh37 |
| NC_000013.9:g.107717494C>G | NCBI36 |
| NG_029524.1:g.2517C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000486502.1:n.78-2955C>G | ||
| XR_931715.1:n.1780C>G |