HGVS | Genome Assembly |
---|---|
NC_000019.10:g.50871716T>A , CM000681.2:g.50871716T>A | GRCh38 |
NC_000019.9:g.51374972T>A , CM000681.1:g.51374972T>A | GRCh37 |
NC_000019.8:g.56066784T>A | NCBI36 |
NG_031984.1:g.3284T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000593493.5:c.-332-1467T>A (KLK2) | ENSP00000472852.1:n.-332-1467T>A | |
ENST00000595375.5:n.149+967T>A (KLK2) | ||
ENST00000596950.5:n.113+859T>A (KLK2) | ||
ENST00000597509.5:n.243+859T>A (KLK2) | ||
XR_935817.1:n.1325-5965T>A (KLK3) |