Linked Data
dbSNP Id:
rs2144568500
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.42470454C>T , CM000680.2:g.42470454C>T | GRCh38 |
| NC_000018.9:g.40050419C>T , CM000680.1:g.40050419C>T | GRCh37 |
| NC_000018.8:g.38304417C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_046174.2:n.872+15465C>T | ||
| NR_046454.1:n.652+15465C>T | ||
| NR_046455.1:n.489+15465C>T |