Linked Data
gnomAD v4:
11-2171900-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2171900C>G , CM000673.2:g.2171900C>G | GRCh38 |
| NC_000011.9:g.2193130C>G , CM000673.1:g.2193130C>G | GRCh37 |
| NC_000011.8:g.2149706C>G | NCBI36 |
| NG_008128.1:g.4906G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011520335.1:c.-114G>C | XP_011518637.1:n.-114G>C | |
| XM_011520335.2:c.-114G>C | XP_011518637.1:n.-114G>C |