Canonical Allele Identifier: CA996823396

Linked Data

dbSNP Id: rs2090232279

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871705C>T , CM000681.2:g.50871705C>T GRCh38
NC_000019.9:g.51374961C>T , CM000681.1:g.51374961C>T GRCh37
NC_000019.8:g.56066773C>T NCBI36
NG_031984.1:g.3273C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1478C>T (KLK2) ENSP00000472852.1:n.-332-1478C>T
ENST00000595375.5:n.149+956C>T (KLK2)
ENST00000596950.5:n.113+848C>T (KLK2)
ENST00000597509.5:n.243+848C>T (KLK2)
XR_935817.1:n.1325-5976C>T (KLK3)