Canonical Allele Identifier: CA14678136

Linked Data

dbSNP Id: rs10424878

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871711A>G , CM000681.2:g.50871711A>G GRCh38
NC_000019.9:g.51374967A>G , CM000681.1:g.51374967A>G GRCh37
NC_000019.8:g.56066779A>G NCBI36
NG_031984.1:g.3279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1472A>G (KLK2) ENSP00000472852.1:n.-332-1472A>G
ENST00000595375.5:n.149+962A>G (KLK2)
ENST00000596950.5:n.113+854A>G (KLK2)
ENST00000597509.5:n.243+854A>G (KLK2)
XR_935817.1:n.1325-5970A>G (KLK3)