Linked Data
dbSNP Id:
rs2047488787
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.73811626T>C , CM000679.2:g.73811626T>C | GRCh38 |
| NC_000017.10:g.71807765T>C , CM000679.1:g.71807765T>C | GRCh37 |
| NC_000017.9:g.69319360T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_027146.1:n.228+12062A>G |