Canonical Allele Identifier: CA309642922

Linked Data

dbSNP Id: rs149689716

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871736T>C , CM000681.2:g.50871736T>C GRCh38
NC_000019.9:g.51374992T>C , CM000681.1:g.51374992T>C GRCh37
NC_000019.8:g.56066804T>C NCBI36
NG_031984.1:g.3304T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1447T>C (KLK2) ENSP00000472852.1:n.-332-1447T>C
ENST00000595375.5:n.149+987T>C (KLK2)
ENST00000596950.5:n.113+879T>C (KLK2)
ENST00000597509.5:n.243+879T>C (KLK2)
XR_935817.1:n.1325-5945T>C (KLK3)