Linked Data
dbSNP Id:
rs1578948784
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.174106391T>A , CM000666.2:g.174106391T>A | GRCh38 |
| NC_000004.11:g.175027542T>A , CM000666.1:g.175027542T>A | GRCh37 |
| NC_000004.10:g.175264117T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125896.1:n.276-8562A>T | ||
| XR_939484.1:n.877+18752T>A | ||
| XR_939485.1:n.877+18752T>A |