Linked Data
dbSNP Id:
rs1727184522
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.38811401G>C , CM000666.2:g.38811401G>C | GRCh38 |
| NC_000004.11:g.38813022G>C , CM000666.1:g.38813022G>C | GRCh37 |
| NC_000004.10:g.38489417G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000506146.5:c.-352-6208C>G | ENSP00000423725.1:n.-352-6208C>G |