Linked Data
dbSNP Id:
rs955893138
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.51936038A>C , CM000664.2:g.51936038A>C | GRCh38 |
| NC_000002.11:g.52163176A>C , CM000664.1:g.52163176A>C | GRCh37 |
| NC_000002.10:g.52016680A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245003.1:n.879+74550A>C | ||
| NR_135237.1:n.879+74550A>C |