Canonical Allele Identifier: CA883227265

Linked Data

dbSNP Id: rs1436838934

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871774G>T , CM000681.2:g.50871774G>T GRCh38
NC_000019.9:g.51375030G>T , CM000681.1:g.51375030G>T GRCh37
NC_000019.8:g.56066842G>T NCBI36
NG_031984.1:g.3342G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1409G>T (KLK2) ENSP00000472852.1:n.-332-1409G>T
ENST00000595375.5:n.149+1025G>T (KLK2)
ENST00000596950.5:n.113+917G>T (KLK2)
ENST00000597509.5:n.243+917G>T (KLK2)
XR_935817.1:n.1325-5907G>T (KLK3)