Linked Data
dbSNP Id:
rs981485112
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.50871690G>A , CM000681.2:g.50871690G>A | GRCh38 |
| NC_000019.9:g.51374946G>A , CM000681.1:g.51374946G>A | GRCh37 |
| NC_000019.8:g.56066758G>A | NCBI36 |
| NG_031984.1:g.3258G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593493.5:c.-332-1493G>A (KLK2) | ENSP00000472852.1:n.-332-1493G>A | |
| ENST00000595375.5:n.149+941G>A (KLK2) | ||
| ENST00000596950.5:n.113+833G>A (KLK2) | ||
| ENST00000597509.5:n.243+833G>A (KLK2) | ||
| XR_935817.1:n.1325-5991G>A (KLK3) |