Linked Data
gnomAD v4:
11-67491150-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67491150G>T , CM000673.2:g.67491150G>T | GRCh38 |
| NC_000011.9:g.67258621G>T , CM000673.1:g.67258621G>T | GRCh37 |
| NC_000011.8:g.67015197G>T | NCBI36 |
| NG_008969.1:g.13117G>T , LRG_460:g.13117G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684657.1:c.*157G>T | ENSP00000507961.1:n.*157G>T |