Linked Data
dbSNP Id:
rs2069697887
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110717605C>T , CM000674.2:g.110717605C>T | GRCh38 |
| NC_000012.11:g.111155410C>T , CM000674.1:g.111155410C>T | GRCh37 |
| NC_000012.10:g.109639793C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011538504.1:c.944-2458G>A | XP_011536806.1:n.944-2458G>A | |
| XM_011538505.1:c.943+3500G>A | XP_011536807.1:n.943+3500G>A | |
| XM_011538504.3:c.944-2458G>A | XP_011536806.1:n.944-2458G>A | |
| XM_011538505.3:c.943+3500G>A | XP_011536807.1:n.943+3500G>A |