Linked Data
dbSNP Id:
rs1780256849
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.7968291T>C , CM000669.2:g.7968291T>C | GRCh38 |
| NC_000007.13:g.8007922T>C , CM000669.1:g.8007922T>C | GRCh37 |
| NC_000007.12:g.7974447T>C | NCBI36 |
| NG_032073.1:g.4549T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110018.1:n.209+253A>G |