Linked Data
dbSNP Id:
rs1830191783
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.99356788C>T , CM000671.2:g.99356788C>T | GRCh38 |
| NC_000009.11:g.102119070C>T , CM000671.1:g.102119070C>T | GRCh37 |
| NC_000009.10:g.101158891C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_102270.1:n.1971-1186G>A | ||
| NR_102271.1:n.1419-1186G>A |