Linked Data
gnomAD v4:
11-2171922-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2171922T>C , CM000673.2:g.2171922T>C | GRCh38 |
| NC_000011.9:g.2193152T>C , CM000673.1:g.2193152T>C | GRCh37 |
| NC_000011.8:g.2149728T>C | NCBI36 |
| NG_008128.1:g.4884A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011520335.1:c.-136A>G | XP_011518637.1:n.-136A>G | |
| XM_011520335.2:c.-136A>G | XP_011518637.1:n.-136A>G |