Canonical Allele Identifier: CA2341121194

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871681T= , CM000681.2:g.50871681T= GRCh38
NC_000019.9:g.51374937T= , CM000681.1:g.51374937T= GRCh37
NC_000019.8:g.56066749T= NCBI36
NG_031984.1:g.3249T=

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1502T= (KLK2) ENSP00000472852.1:n.-332-1502T=
ENST00000595375.5:n.149+932T= (KLK2)
ENST00000596950.5:n.113+824T= (KLK2)
ENST00000597509.5:n.243+824T= (KLK2)
XR_935817.1:n.1325-6000T= (KLK3)