Linked Data
gnomAD v4:
11-67483007-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67483007A>G , CM000673.2:g.67483007A>G | GRCh38 |
| NC_000011.9:g.67250478A>G , CM000673.1:g.67250478A>G | GRCh37 |
| NC_000011.8:g.67007054A>G | NCBI36 |
| NG_008969.1:g.4974A>G , LRG_460:g.4974A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682699.1:c.-152A>G | ENSP00000507935.1:n.-152A>G | |
| XM_024448761.1:c.-152A>G | XP_024304529.1:n.-152A>G |