Canonical Allele Identifier: CA883227295

Linked Data

dbSNP Id: rs1447667984

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871798G>A , CM000681.2:g.50871798G>A GRCh38
NC_000019.9:g.51375054G>A , CM000681.1:g.51375054G>A GRCh37
NC_000019.8:g.56066866G>A NCBI36
NG_031984.1:g.3366G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1385G>A (KLK2) ENSP00000472852.1:n.-332-1385G>A
ENST00000595375.5:n.149+1049G>A (KLK2)
ENST00000596950.5:n.113+941G>A (KLK2)
ENST00000597509.5:n.243+941G>A (KLK2)
XR_935817.1:n.1325-5883G>A (KLK3)