Linked Data
dbSNP Id:
rs2066912009
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097983C>A , CM000685.2:g.154097983C>A | GRCh38 |
| NC_000023.10:g.153363441C>A , CM000685.1:g.153363441C>A | GRCh37 |
| NC_000023.9:g.153016635C>A | NCBI36 |
| NG_007107.2:g.44138G>T | |
| NG_007107.3:g.44121G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000631210.1:n.305+6798G>T |