Linked Data
dbSNP Id:
rs1780638062
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32634786A>T , CM000668.2:g.32634786A>T | GRCh38 |
| NC_000006.11:g.32602563A>T , CM000668.1:g.32602563A>T | GRCh37 |
| NC_000006.10:g.32710541A>T | NCBI36 |
| NG_032876.1:g.2381A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000422863.1:c.-39+1877A>T | ENSP00000405797.1:n.-39+1877A>T |