Linked Data
dbSNP Id:
rs566094718
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.104379338G>A , CM000670.2:g.104379338G>A | GRCh38 |
| NC_000008.10:g.105391566G>A , CM000670.1:g.105391566G>A | GRCh37 |
| NC_000008.9:g.105460742G>A | NCBI36 |
| NG_008840.1:g.92712C>T | |
| NG_008840.2:g.92712C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521601.1:n.328+1846C>T |