Canonical Allele Identifier: CA2341121195

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871682C= , CM000681.2:g.50871682C= GRCh38
NC_000019.9:g.51374938C= , CM000681.1:g.51374938C= GRCh37
NC_000019.8:g.56066750C= NCBI36
NG_031984.1:g.3250C=

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1501C= (KLK2) ENSP00000472852.1:n.-332-1501C=
ENST00000595375.5:n.149+933C= (KLK2)
ENST00000596950.5:n.113+825C= (KLK2)
ENST00000597509.5:n.243+825C= (KLK2)
XR_935817.1:n.1325-5999C= (KLK3)