Linked Data
dbSNP Id:
rs1369724851
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.220836657G>T , CM000663.2:g.220836657G>T | GRCh38 |
| NC_000001.10:g.221009999G>T , CM000663.1:g.221009999G>T | GRCh37 |
| NC_000001.9:g.219076622G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651706.1:c.842+31383G>T | ENSP00000499157.1:n.842+31383G>T | |
| NR_046901.1:n.293-3465C>A |