Linked Data
dbSNP Id:
rs1568996768
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.35641406A>G , CM000683.2:g.35641406A>G | GRCh38 |
| NC_000021.8:g.37013704A>G , CM000683.1:g.37013704A>G | GRCh37 |
| NC_000021.7:g.35935574A>G | NCBI36 |
| NG_011402.2:g.348305T>C , LRG_482:g.348305T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475045.6:c.-532+13414T>C | ENSP00000477072.1:n.-532+13414T>C |