Linked Data
dbSNP Id:
rs1858267556
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798477A>C , CM000673.2:g.102798477A>C | GRCh38 |
| NC_000011.9:g.102669208A>C , CM000673.1:g.102669208A>C | GRCh37 |
| NC_000011.8:g.102174418A>C | NCBI36 |
| NG_011740.1:g.4759T>G | |
| NG_011740.2:g.4759T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371455.7:n.423+355A>C | ||
| ENST00000525739.6:n.682+355A>C | ||
| ENST00000544704.1:n.443+355A>C | ||
| NR_038390.1:n.682+355A>C |