Canonical Allele Identifier: CA2341121180

Linked Data

dbSNP Id: rs2090231758

Genomic Alleles

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

Transcript Alleles

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