Linked Data
dbSNP Id:
rs1756295817
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79111488C>T , CM000667.2:g.79111488C>T | GRCh38 |
| NC_000005.9:g.78407311C>T , CM000667.1:g.78407311C>T | GRCh37 |
| NC_000005.8:g.78443067C>T | NCBI36 |
| NG_029156.1:g.4708C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000520388.5:n.492-7210G>A |