Linked Data
dbSNP Id:
rs550349966
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110717803T>G , CM000674.2:g.110717803T>G | GRCh38 |
| NC_000012.11:g.111155608T>G , CM000674.1:g.111155608T>G | GRCh37 |
| NC_000012.10:g.109639991T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011538504.1:c.944-2656A>C | XP_011536806.1:n.944-2656A>C | |
| XM_011538505.1:c.943+3302A>C | XP_011536807.1:n.943+3302A>C | |
| XM_011538504.3:c.944-2656A>C | XP_011536806.1:n.944-2656A>C | |
| XM_011538505.3:c.943+3302A>C | XP_011536807.1:n.943+3302A>C |