Linked Data
gnomAD v4:
6-32390441-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32390441T>C , CM000668.2:g.32390441T>C | GRCh38 |
| NC_000006.11:g.32358218T>C , CM000668.1:g.32358218T>C | GRCh37 |
| NC_000006.10:g.32466196T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011515039.1:c.482-15013T>C | XP_011513341.1:n.482-15013T>C | |
| NR_136245.1:n.303-15013T>C |