Linked Data
dbSNP Id:
rs1433230100
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47402982T>G , CM000664.2:g.47402982T>G | GRCh38 |
| NC_000002.11:g.47630121T>G , CM000664.1:g.47630121T>G | GRCh37 |
| NC_000002.10:g.47483625T>G | NCBI36 |
| NG_007110.2:g.4859T>G , LRG_218:g.4859T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233146.6:c.-210T>G | ENSP00000233146.2:n.-210T>G |