Canonical Allele Identifier: CA309642854

Linked Data

dbSNP Id: rs1055854093

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871652A>G , CM000681.2:g.50871652A>G GRCh38
NC_000019.9:g.51374908A>G , CM000681.1:g.51374908A>G GRCh37
NC_000019.8:g.56066720A>G NCBI36
NG_031984.1:g.3220A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1531A>G (KLK2) ENSP00000472852.1:n.-332-1531A>G
ENST00000595375.5:n.149+903A>G (KLK2)
ENST00000596950.5:n.113+795A>G (KLK2)
ENST00000597509.5:n.243+795A>G (KLK2)
XR_935817.1:n.1325-6029A>G (KLK3)