Linked Data
dbSNP Id:
rs1858266100
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798404C>A , CM000673.2:g.102798404C>A | GRCh38 |
| NC_000011.9:g.102669135C>A , CM000673.1:g.102669135C>A | GRCh37 |
| NC_000011.8:g.102174345C>A | NCBI36 |
| NG_011740.1:g.4832G>T | |
| NG_011740.2:g.4832G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371455.7:n.423+282C>A | ||
| ENST00000525739.6:n.682+282C>A | ||
| ENST00000544704.1:n.443+282C>A | ||
| NR_038390.1:n.682+282C>A |