Linked Data
dbSNP Id:
rs1839809182
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44385980G>C , CM000672.2:g.44385980G>C | GRCh38 |
| NC_000010.10:g.44881428G>C , CM000672.1:g.44881428G>C | GRCh37 |
| NC_000010.9:g.44201434G>C | NCBI36 |
| NG_016861.1:g.4118C>G | |
| NG_016861.2:g.4118C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496375.1:n.514C>G |