Linked Data
dbSNP Id:
rs1727179136
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.38811092C>T , CM000666.2:g.38811092C>T | GRCh38 |
| NC_000004.11:g.38812713C>T , CM000666.1:g.38812713C>T | GRCh37 |
| NC_000004.10:g.38489108C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000506146.5:c.-352-5899G>A | ENSP00000423725.1:n.-352-5899G>A |