Linked Data
dbSNP Id:
rs1446543596
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203866172C>T , CM000664.2:g.203866172C>T | GRCh38 |
| NC_000002.11:g.204730895C>T , CM000664.1:g.204730895C>T | GRCh37 |
| NC_000002.10:g.204439140C>T | NCBI36 |
| NG_011502.1:g.3387C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696479.1:c.48-1746C>T | ENSP00000512655.1:n.48-1746C>T |