Linked Data
gnomAD v4:
11-2171855-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2171855A>G , CM000673.2:g.2171855A>G | GRCh38 |
| NC_000011.9:g.2193085A>G , CM000673.1:g.2193085A>G | GRCh37 |
| NC_000011.8:g.2149661A>G | NCBI36 |
| NG_008128.1:g.4951T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000352909.7:c.-69T>C | ENSP00000325951.3:n.-69T>C | |
| XM_011520335.1:c.-69T>C | XP_011518637.1:n.-69T>C | |
| XM_011520335.2:c.-69T>C | XP_011518637.1:n.-69T>C |