Linked Data
gnomAD v4:
11-67482993-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67482993G>T , CM000673.2:g.67482993G>T | GRCh38 |
| NC_000011.9:g.67250464G>T , CM000673.1:g.67250464G>T | GRCh37 |
| NC_000011.8:g.67007040G>T | NCBI36 |
| NG_008969.1:g.4960G>T , LRG_460:g.4960G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682699.1:c.-166G>T | ENSP00000507935.1:n.-166G>T | |
| XM_024448761.1:c.-166G>T | XP_024304529.1:n.-166G>T |