Canonical Allele Identifier: CA2341121190

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871673T= , CM000681.2:g.50871673T= GRCh38
NC_000019.9:g.51374929T= , CM000681.1:g.51374929T= GRCh37
NC_000019.8:g.56066741T= NCBI36
NG_031984.1:g.3241T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1510T= (KLK2) ENSP00000472852.1:n.-332-1510T=
ENST00000595375.5:n.149+924T= (KLK2)
ENST00000596950.5:n.113+816T= (KLK2)
ENST00000597509.5:n.243+816T= (KLK2)
XR_935817.1:n.1325-6008T= (KLK3)