Linked Data
gnomAD v4:
11-67491143-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67491143A>C , CM000673.2:g.67491143A>C | GRCh38 |
| NC_000011.9:g.67258614A>C , CM000673.1:g.67258614A>C | GRCh37 |
| NC_000011.8:g.67015190A>C | NCBI36 |
| NG_008969.1:g.13110A>C , LRG_460:g.13110A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684657.1:c.*150A>C | ENSP00000507961.1:n.*150A>C |