Linked Data
dbSNP Id:
rs2118179927
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99356810G>C , CM000671.2:g.99356810G>C | GRCh38 |
| NC_000009.11:g.102119092G>C , CM000671.1:g.102119092G>C | GRCh37 |
| NC_000009.10:g.101158913G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_102270.1:n.1971-1208C>G | ||
| NR_102271.1:n.1419-1208C>G |