Linked Data
dbSNP Id:
rs2055056892
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.26866288C>T , CM000680.2:g.26866288C>T | GRCh38 |
| NC_000018.9:g.24446252C>T , CM000680.1:g.24446252C>T | GRCh37 |
| NC_000018.8:g.22700250C>T | NCBI36 |
| NG_029560.1:g.4465G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_026908.1:n.53+928C>T |