Canonical Allele Identifier: CA309642863

Linked Data

dbSNP Id: rs573998526

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871678A>G , CM000681.2:g.50871678A>G GRCh38
NC_000019.9:g.51374934A>G , CM000681.1:g.51374934A>G GRCh37
NC_000019.8:g.56066746A>G NCBI36
NG_031984.1:g.3246A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1505A>G (KLK2) ENSP00000472852.1:n.-332-1505A>G
ENST00000595375.5:n.149+929A>G (KLK2)
ENST00000596950.5:n.113+821A>G (KLK2)
ENST00000597509.5:n.243+821A>G (KLK2)
XR_935817.1:n.1325-6003A>G (KLK3)