Linked Data
dbSNP Id:
rs1909606282
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.24460610A>C , CM000680.2:g.24460610A>C | GRCh38 |
| NC_000018.9:g.22040574A>C , CM000680.1:g.22040574A>C | GRCh37 |
| NC_000018.8:g.20294572A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011526133.1:c.-119A>C | XP_011524435.1:n.-119A>C | |
| XM_011526134.1:c.-119A>C | XP_011524436.1:n.-119A>C |