Canonical Allele Identifier: CA883227184

Linked Data

dbSNP Id: rs1458671639

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871670G>T , CM000681.2:g.50871670G>T GRCh38
NC_000019.9:g.51374926G>T , CM000681.1:g.51374926G>T GRCh37
NC_000019.8:g.56066738G>T NCBI36
NG_031984.1:g.3238G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1513G>T (KLK2) ENSP00000472852.1:n.-332-1513G>T
ENST00000595375.5:n.149+921G>T (KLK2)
ENST00000596950.5:n.113+813G>T (KLK2)
ENST00000597509.5:n.243+813G>T (KLK2)
XR_935817.1:n.1325-6011G>T (KLK3)