Linked Data
gnomAD v4:
6-32390446-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390446C>T , CM000668.2:g.32390446C>T | GRCh38 |
| NC_000006.11:g.32358223C>T , CM000668.1:g.32358223C>T | GRCh37 |
| NC_000006.10:g.32466201C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011515039.1:c.482-15008C>T | XP_011513341.1:n.482-15008C>T | |
| NR_136245.1:n.303-15008C>T |