HGVS | Genome Assembly |
---|---|
NC_000019.10:g.50871662T>G , CM000681.2:g.50871662T>G | GRCh38 |
NC_000019.9:g.51374918T>G , CM000681.1:g.51374918T>G | GRCh37 |
NC_000019.8:g.56066730T>G | NCBI36 |
NG_031984.1:g.3230T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000593493.5:c.-332-1521T>G (KLK2) | ENSP00000472852.1:n.-332-1521T>G | |
ENST00000595375.5:n.149+913T>G (KLK2) | ||
ENST00000596950.5:n.113+805T>G (KLK2) | ||
ENST00000597509.5:n.243+805T>G (KLK2) | ||
XR_935817.1:n.1325-6019T>G (KLK3) |