Linked Data
dbSNP Id:
rs1858750923
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1100041T>C , CM000673.2:g.1100041T>C | GRCh38 |
| NC_000011.9:g.1093949T>C , CM000673.1:g.1093949T>C | GRCh37 |
| NC_000011.8:g.1083949T>C | NCBI36 |
| NG_051929.1:g.32068T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000361558.7:n.9809+16T>C | ||
| ENST00000674892.1:c.256+16T>C | ENSP00000501871.1:n.256+16T>C |