Linked Data
dbSNP Id:
rs2109455558
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55346116G>A , CM000666.2:g.55346116G>A | GRCh38 |
| NC_000004.11:g.56212283G>A , CM000666.1:g.56212283G>A | GRCh37 |
| NC_000004.10:g.55907040G>A | NCBI36 |
| NG_028230.1:g.4896G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264228.8:c.-221G>A | ENSP00000264228.4:n.-221G>A |