Linked Data
dbSNP Id:
rs1688626846
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203866277T>A , CM000664.2:g.203866277T>A | GRCh38 |
| NC_000002.11:g.204731000T>A , CM000664.1:g.204731000T>A | GRCh37 |
| NC_000002.10:g.204439245T>A | NCBI36 |
| NG_011502.1:g.3492T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696479.1:c.48-1641T>A | ENSP00000512655.1:n.48-1641T>A |