Linked Data
dbSNP Id:
rs17885289
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.44386212C>G , CM000672.2:g.44386212C>G | GRCh38 |
| NC_000010.10:g.44881660C>G , CM000672.1:g.44881660C>G | GRCh37 |
| NC_000010.9:g.44201666C>G | NCBI36 |
| NG_016861.1:g.3886G>C | |
| NG_016861.2:g.3886G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000496375.1:n.282G>C |