Canonical Allele Identifier: CA309642952

Linked Data

dbSNP Id: rs920163825

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871752C>T , CM000681.2:g.50871752C>T GRCh38
NC_000019.9:g.51375008C>T , CM000681.1:g.51375008C>T GRCh37
NC_000019.8:g.56066820C>T NCBI36
NG_031984.1:g.3320C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1431C>T (KLK2) ENSP00000472852.1:n.-332-1431C>T
ENST00000595375.5:n.149+1003C>T (KLK2)
ENST00000596950.5:n.113+895C>T (KLK2)
ENST00000597509.5:n.243+895C>T (KLK2)
XR_935817.1:n.1325-5929C>T (KLK3)