Linked Data
dbSNP Id:
rs1159798137
gnomAD v3:
11-14894160-C-G
gnomAD v4:
11-14894160-C-G
MyVariant Identifiers:
chr11:g.14894160C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14894160C>G , CM000673.2:g.14894160C>G | GRCh38 |
| NC_000011.9:g.14915706C>G , CM000673.1:g.14915706C>G | GRCh37 |
| NC_000011.8:g.14872282C>G | NCBI36 |
| NG_007936.1:g.3046G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.3:c.-1916G>C | XP_011518200.1:n.-1916G>C |