Canonical Allele Identifier: CA883227183

Linked Data

dbSNP Id: rs1159621290

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871668G>A , CM000681.2:g.50871668G>A GRCh38
NC_000019.9:g.51374924G>A , CM000681.1:g.51374924G>A GRCh37
NC_000019.8:g.56066736G>A NCBI36
NG_031984.1:g.3236G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1515G>A (KLK2) ENSP00000472852.1:n.-332-1515G>A
ENST00000595375.5:n.149+919G>A (KLK2)
ENST00000596950.5:n.113+811G>A (KLK2)
ENST00000597509.5:n.243+811G>A (KLK2)
XR_935817.1:n.1325-6013G>A (KLK3)