Linked Data
dbSNP Id:
rs1858266878
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798436A>G , CM000673.2:g.102798436A>G | GRCh38 |
| NC_000011.9:g.102669167A>G , CM000673.1:g.102669167A>G | GRCh37 |
| NC_000011.8:g.102174377A>G | NCBI36 |
| NG_011740.1:g.4800T>C | |
| NG_011740.2:g.4800T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371455.7:n.423+314A>G | ||
| ENST00000525739.6:n.682+314A>G | ||
| ENST00000544704.1:n.443+314A>G | ||
| NR_038390.1:n.682+314A>G |