Linked Data
dbSNP Id:
rs2130119266
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2982863C>G , CM000671.2:g.2982863C>G | GRCh38 |
| NC_000009.11:g.2982863C>G , CM000671.1:g.2982863C>G | GRCh37 |
| NC_000009.10:g.2972863C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426329.6:n.427+9600G>C |