Linked Data
dbSNP Id:
rs1780613391
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32634458T>A , CM000668.2:g.32634458T>A | GRCh38 |
| NC_000006.11:g.32602235T>A , CM000668.1:g.32602235T>A | GRCh37 |
| NC_000006.10:g.32710213T>A | NCBI36 |
| NG_032876.1:g.2053T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000422863.1:c.-39+1549T>A | ENSP00000405797.1:n.-39+1549T>A |