Canonical Allele Identifier: CA633706692

Linked Data

dbSNP Id: rs981485112

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871690G>C , CM000681.2:g.50871690G>C GRCh38
NC_000019.9:g.51374946G>C , CM000681.1:g.51374946G>C GRCh37
NC_000019.8:g.56066758G>C NCBI36
NG_031984.1:g.3258G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1493G>C (KLK2) ENSP00000472852.1:n.-332-1493G>C
ENST00000595375.5:n.149+941G>C (KLK2)
ENST00000596950.5:n.113+833G>C (KLK2)
ENST00000597509.5:n.243+833G>C (KLK2)
XR_935817.1:n.1325-5991G>C (KLK3)