Linked Data
dbSNP Id:
rs11771145
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143413669G>T , CM000669.2:g.143413669G>T | GRCh38 |
| NC_000007.13:g.143110762G>T , CM000669.1:g.143110762G>T | GRCh37 |
| NC_000007.12:g.142820884G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_033897.1:n.75-1399G>T |