Canonical Allele Identifier: CA2559042508

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871758C>T , CM000681.2:g.50871758C>T GRCh38
NC_000019.9:g.51375014C>T , CM000681.1:g.51375014C>T GRCh37
NC_000019.8:g.56066826C>T NCBI36
NG_031984.1:g.3326C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1425C>T (KLK2) ENSP00000472852.1:n.-332-1425C>T
ENST00000595375.5:n.149+1009C>T (KLK2)
ENST00000596950.5:n.113+901C>T (KLK2)
ENST00000597509.5:n.243+901C>T (KLK2)
XR_935817.1:n.1325-5923C>T (KLK3)