Linked Data
dbSNP Id:
rs1020689958
gnomAD v3:
12-110717404-C-G
gnomAD v4:
12-110717404-C-G
MyVariant Identifiers:
chr12:g.110717404C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.110717404C>G , CM000674.2:g.110717404C>G | GRCh38 |
| NC_000012.11:g.111155209C>G , CM000674.1:g.111155209C>G | GRCh37 |
| NC_000012.10:g.109639592C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011538504.1:c.944-2257G>C | XP_011536806.1:n.944-2257G>C | |
| XM_011538505.1:c.943+3701G>C | XP_011536807.1:n.943+3701G>C | |
| XM_011538504.3:c.944-2257G>C | XP_011536806.1:n.944-2257G>C | |
| XM_011538505.3:c.943+3701G>C | XP_011536807.1:n.943+3701G>C |