Linked Data
dbSNP Id:
rs2129959532
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118960491A>G , CM000670.2:g.118960491A>G | GRCh38 |
| NC_000008.10:g.119972730A>G , CM000670.1:g.119972730A>G | GRCh37 |
| NC_000008.9:g.120041911A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_005250756.2:c.-60+8113A>G | XP_005250813.1:n.-60+8113A>G | |
| NM_001324095.1:c.-324+8113A>G | NP_001311024.1:n.-324+8113A>G | |
| XM_005250756.3:c.-60+8113A>G | XP_005250813.1:n.-60+8113A>G | |
| NM_001324095.2:c.-324+8113A>G | NP_001311024.1:n.-324+8113A>G |