Canonical Allele Identifier: CA2341121179

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871653T= , CM000681.2:g.50871653T= GRCh38
NC_000019.9:g.51374909T= , CM000681.1:g.51374909T= GRCh37
NC_000019.8:g.56066721T= NCBI36
NG_031984.1:g.3221T=

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1530T= (KLK2) ENSP00000472852.1:n.-332-1530T=
ENST00000595375.5:n.149+904T= (KLK2)
ENST00000596950.5:n.113+796T= (KLK2)
ENST00000597509.5:n.243+796T= (KLK2)
XR_935817.1:n.1325-6028T= (KLK3)