Linked Data
gnomAD v4:
11-67483002-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67483002T>A , CM000673.2:g.67483002T>A | GRCh38 |
| NC_000011.9:g.67250473T>A , CM000673.1:g.67250473T>A | GRCh37 |
| NC_000011.8:g.67007049T>A | NCBI36 |
| NG_008969.1:g.4969T>A , LRG_460:g.4969T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682699.1:c.-157T>A | ENSP00000507935.1:n.-157T>A | |
| XM_024448761.1:c.-157T>A | XP_024304529.1:n.-157T>A |