Linked Data
dbSNP Id:
rs572639038
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72134421C>A , CM000673.2:g.72134421C>A | GRCh38 |
| NC_000011.9:g.71845467C>A , CM000673.1:g.71845467C>A | GRCh37 |
| NC_000011.8:g.71523115C>A | NCBI36 |
| NG_032935.1:g.3697C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622388.4:c.-6-1526C>A | ENSP00000481833.1:n.-6-1526C>A |