Canonical Allele Identifier: CA883227242

Linked Data

dbSNP Id: rs1209608264

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871707T>C , CM000681.2:g.50871707T>C GRCh38
NC_000019.9:g.51374963T>C , CM000681.1:g.51374963T>C GRCh37
NC_000019.8:g.56066775T>C NCBI36
NG_031984.1:g.3275T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1476T>C (KLK2) ENSP00000472852.1:n.-332-1476T>C
ENST00000595375.5:n.149+958T>C (KLK2)
ENST00000596950.5:n.113+850T>C (KLK2)
ENST00000597509.5:n.243+850T>C (KLK2)
XR_935817.1:n.1325-5974T>C (KLK3)