Linked Data
gnomAD v4:
11-67491149-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67491149T>A , CM000673.2:g.67491149T>A | GRCh38 |
| NC_000011.9:g.67258620T>A , CM000673.1:g.67258620T>A | GRCh37 |
| NC_000011.8:g.67015196T>A | NCBI36 |
| NG_008969.1:g.13116T>A , LRG_460:g.13116T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684657.1:c.*156T>A | ENSP00000507961.1:n.*156T>A |