Linked Data
dbSNP Id:
rs1186737140
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.84458137G>T , CM000675.2:g.84458137G>T | GRCh38 |
| NC_000013.10:g.85032272G>T , CM000675.1:g.85032272G>T | GRCh37 |
| NC_000013.9:g.83930273G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_046871.1:n.139-104227G>T | ||
| XR_942133.1:n.369-46218C>A | ||
| XR_942134.1:n.366-46218C>A |