Linked Data
dbSNP Id:
rs1718767766
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.77215857T>C , CM000666.2:g.77215857T>C | GRCh38 |
| NC_000004.11:g.78137010T>C , CM000666.1:g.78137010T>C | GRCh37 |
| NC_000004.10:g.78356034T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000497512.5:n.1675+23590T>C | ||
| ENST00000514756.1:n.101+23590T>C |