Linked Data
dbSNP Id:
rs1646766598
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.47388981T>G , CM000663.2:g.47388981T>G | GRCh38 |
| NC_000001.10:g.47854653T>G , CM000663.1:g.47854653T>G | GRCh37 |
| NC_000001.9:g.47627240T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699074.1:c.550-5300T>G (CMPK1) | ENSP00000514113.1:n.550-5300T>G | |
| NR_126355.1:n.405-2625A>C (LINC01389) |