Linked Data
dbSNP Id:
rs2115659993
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.90008222T>C , CM000669.2:g.90008222T>C | GRCh38 |
| NC_000007.13:g.89637536T>C , CM000669.1:g.89637536T>C | GRCh37 |
| NC_000007.12:g.89475472T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_110029.2:n.425-125667A>G |