Canonical Allele Identifier: CA2341121250

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871797T= , CM000681.2:g.50871797T= GRCh38
NC_000019.9:g.51375053T= , CM000681.1:g.51375053T= GRCh37
NC_000019.8:g.56066865T= NCBI36
NG_031984.1:g.3365T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1386T= (KLK2) ENSP00000472852.1:n.-332-1386T=
ENST00000595375.5:n.149+1048T= (KLK2)
ENST00000596950.5:n.113+940T= (KLK2)
ENST00000597509.5:n.243+940T= (KLK2)
XR_935817.1:n.1325-5884T= (KLK3)