Linked Data
dbSNP Id:
rs1820172059
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.129465564T>C , CM000670.2:g.129465564T>C | GRCh38 |
| NC_000008.10:g.130477810T>C , CM000670.1:g.130477810T>C | GRCh37 |
| NC_000008.9:g.130546992T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_130917.1:n.360+15079A>G | ||
| NR_130918.1:n.138-95187A>G | ||
| NR_130919.1:n.138-65880A>G | ||
| NR_130920.1:n.138-65880A>G |