Linked Data
gnomAD v4:
11-67491132-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67491132A>G , CM000673.2:g.67491132A>G | GRCh38 |
| NC_000011.9:g.67258603A>G , CM000673.1:g.67258603A>G | GRCh37 |
| NC_000011.8:g.67015179A>G | NCBI36 |
| NG_008969.1:g.13099A>G , LRG_460:g.13099A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684657.1:c.*139A>G | ENSP00000507961.1:n.*139A>G |