Canonical Allele Identifier: CA996823393

Linked Data

dbSNP Id: rs2090232131

Genomic Alleles

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

Transcript Alleles

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