Linked Data
dbSNP Id:
rs1667130829
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31583871C>T , CM000664.2:g.31583871C>T | GRCh38 |
| NC_000002.11:g.31808940C>T , CM000664.1:g.31808940C>T | GRCh37 |
| NC_000002.10:g.31662444C>T | NCBI36 |
| NG_008365.1:g.2101G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011533070.1:c.27-50105G>A | XP_011531372.1:n.27-50105G>A | |
| XM_011533071.1:c.27-50105G>A | XP_011531373.1:n.27-50105G>A | |
| XM_011533072.1:c.27-50105G>A | XP_011531374.1:n.27-50105G>A | |
| XM_011533072.2:c.27-50105G>A | XP_011531374.1:n.27-50105G>A |