Linked Data
dbSNP Id:
rs2135110268
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62991162T>C , CM000673.2:g.62991162T>C | GRCh38 |
| NC_000011.9:g.62758634T>C , CM000673.1:g.62758634T>C | GRCh37 |
| NC_000011.8:g.62515210T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539841.1:n.5570A>G |