Canonical Allele Identifier: CA309642953

Linked Data

dbSNP Id: rs565295156

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871782C>A , CM000681.2:g.50871782C>A GRCh38
NC_000019.9:g.51375038C>A , CM000681.1:g.51375038C>A GRCh37
NC_000019.8:g.56066850C>A NCBI36
NG_031984.1:g.3350C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1401C>A (KLK2) ENSP00000472852.1:n.-332-1401C>A
ENST00000595375.5:n.149+1033C>A (KLK2)
ENST00000596950.5:n.113+925C>A (KLK2)
ENST00000597509.5:n.243+925C>A (KLK2)
XR_935817.1:n.1325-5899C>A (KLK3)