Linked Data
dbSNP Id:
rs1281072484
gnomAD v3:
11-14893536-G-C
gnomAD v4:
11-14893536-G-C
MyVariant Identifiers:
chr11:g.14893536G>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.14893536G>C , CM000673.2:g.14893536G>C | GRCh38 |
| NC_000011.9:g.14915082G>C , CM000673.1:g.14915082G>C | GRCh37 |
| NC_000011.8:g.14871658G>C | NCBI36 |
| NG_007936.1:g.3670C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011519898.1:c.-1292C>G | XP_011518200.1:n.-1292C>G | |
| XM_011519898.3:c.-1292C>G | XP_011518200.1:n.-1292C>G |