Linked Data
dbSNP Id:
rs2109068462
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24794766C>A , CM000666.2:g.24794766C>A | GRCh38 |
| NC_000004.11:g.24796388C>A , CM000666.1:g.24796388C>A | GRCh37 |
| NC_000004.10:g.24405486C>A | NCBI36 |
| NG_012213.1:g.4304C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000598411.1:c.-17+4664C>A | ENSP00000472134.1:n.-17+4664C>A |