Linked Data
dbSNP Id:
rs2143094181
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.69854907C>T , CM000679.2:g.69854907C>T | GRCh38 |
| NC_000017.10:g.67851048C>T , CM000679.1:g.67851048C>T | GRCh37 |
| NC_000017.9:g.65362643C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_109971.1:n.363+9421C>T | ||
| NR_109972.1:n.363+9421C>T |