Linked Data
dbSNP Id:
rs1688627314
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.203866283A>G , CM000664.2:g.203866283A>G | GRCh38 |
| NC_000002.11:g.204731006A>G , CM000664.1:g.204731006A>G | GRCh37 |
| NC_000002.10:g.204439251A>G | NCBI36 |
| NG_011502.1:g.3498A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696479.1:c.48-1635A>G | ENSP00000512655.1:n.48-1635A>G |