Linked Data
gnomAD v4:
11-2171887-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2171887C>A , CM000673.2:g.2171887C>A | GRCh38 |
| NC_000011.9:g.2193117C>A , CM000673.1:g.2193117C>A | GRCh37 |
| NC_000011.8:g.2149693C>A | NCBI36 |
| NG_008128.1:g.4919G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011520335.1:c.-101G>T | XP_011518637.1:n.-101G>T | |
| XM_011520335.2:c.-101G>T | XP_011518637.1:n.-101G>T |