Canonical Allele Identifier: CA2341121186

Linked Data

dbSNP Id: rs915686423

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871657G>T , CM000681.2:g.50871657G>T GRCh38
NC_000019.9:g.51374913G>T , CM000681.1:g.51374913G>T GRCh37
NC_000019.8:g.56066725G>T NCBI36
NG_031984.1:g.3225G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1526G>T (KLK2) ENSP00000472852.1:n.-332-1526G>T
ENST00000595375.5:n.149+908G>T (KLK2)
ENST00000596950.5:n.113+800G>T (KLK2)
ENST00000597509.5:n.243+800G>T (KLK2)
XR_935817.1:n.1325-6024G>T (KLK3)