Canonical Allele Identifier: CA2341121206

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871716T= , CM000681.2:g.50871716T= GRCh38
NC_000019.9:g.51374972T= , CM000681.1:g.51374972T= GRCh37
NC_000019.8:g.56066784T= NCBI36
NG_031984.1:g.3284T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1467T= (KLK2) ENSP00000472852.1:n.-332-1467T=
ENST00000595375.5:n.149+967T= (KLK2)
ENST00000596950.5:n.113+859T= (KLK2)
ENST00000597509.5:n.243+859T= (KLK2)
XR_935817.1:n.1325-5965T= (KLK3)