HGVS | Genome Assembly |
---|---|
NC_000019.10:g.50871670G>T , CM000681.2:g.50871670G>T | GRCh38 |
NC_000019.9:g.51374926G>T , CM000681.1:g.51374926G>T | GRCh37 |
NC_000019.8:g.56066738G>T | NCBI36 |
NG_031984.1:g.3238G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000593493.5:c.-332-1513G>T (KLK2) | ENSP00000472852.1:n.-332-1513G>T | |
ENST00000595375.5:n.149+921G>T (KLK2) | ||
ENST00000596950.5:n.113+813G>T (KLK2) | ||
ENST00000597509.5:n.243+813G>T (KLK2) | ||
XR_935817.1:n.1325-6011G>T (KLK3) |