Canonical Allele Identifier: CA2550608490

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871660C>A , CM000681.2:g.50871660C>A GRCh38
NC_000019.9:g.51374916C>A , CM000681.1:g.51374916C>A GRCh37
NC_000019.8:g.56066728C>A NCBI36
NG_031984.1:g.3228C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1523C>A (KLK2) ENSP00000472852.1:n.-332-1523C>A
ENST00000595375.5:n.149+911C>A (KLK2)
ENST00000596950.5:n.113+803C>A (KLK2)
ENST00000597509.5:n.243+803C>A (KLK2)
XR_935817.1:n.1325-6021C>A (KLK3)