Linked Data
gnomAD v4:
5-132369521-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132369521C>T , CM000667.2:g.132369521C>T | GRCh38 |
| NC_000005.9:g.131705213C>T , CM000667.1:g.131705213C>T | GRCh37 |
| NC_000005.8:g.131733112C>T | NCBI36 |
| NG_008982.1:g.4813C>T | |
| NG_008982.2:g.4818C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110997.1:n.73+323G>A |