Linked Data
dbSNP Id:
rs7763822
gnomAD v2:
6-33060428-C-T
gnomAD v3:
6-33092651-C-T
gnomAD v4:
6-33092651-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33092651C>T , CM000668.2:g.33092651C>T | GRCh38 |
| NC_000006.11:g.33060428C>T , CM000668.1:g.33060428C>T | GRCh37 |
| NC_000006.10:g.33168406C>T | NCBI36 |
| NG_033242.1:g.21726C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000433582.1:n.300+242G>A |