Linked Data
gnomAD v4:
4-177442621-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442621C>T , CM000666.2:g.177442621C>T | GRCh38 |
| NC_000004.11:g.178363775C>T , CM000666.1:g.178363775C>T | GRCh37 |
| NC_000004.10:g.178600769C>T | NCBI36 |
| NG_011845.2:g.4883G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741929.1:n.82+40C>T |