Linked Data
gnomAD v4:
6-32644427-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32644427G>T , CM000668.2:g.32644427G>T | GRCh38 |
| NC_000006.11:g.32612204G>T , CM000668.1:g.32612204G>T | GRCh37 |
| NC_000006.10:g.32720182G>T | NCBI36 |
| NG_032876.1:g.12022G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000460633.1:n.2815G>T | ||
| XM_006715079.2:c.613+2174G>T | XP_006715142.1:n.613+2174G>T | |
| XM_006715079.4:c.613+2174G>T | XP_006715142.1:n.613+2174G>T |