Linked Data
dbSNP Id:
rs1846010717
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2444970C>G , CM000673.2:g.2444970C>G | GRCh38 |
| NC_000011.9:g.2466200C>G , CM000673.1:g.2466200C>G | GRCh37 |
| NC_000011.8:g.2422776C>G | NCBI36 |
| NG_008935.1:g.4980C>G , LRG_287:g.4980C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.23+262C>G | ENSP00000434560.2:n.23+262C>G | |
| ENST00000496887.6:c.23+262C>G | ENSP00000434560.1:n.23+262C>G |