Canonical Allele Identifier: CA996823398

Linked Data

dbSNP Id: rs2090232333

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871709dup , CM000681.2:g.50871709dup GRCh38
NC_000019.9:g.51374965dup , CM000681.1:g.51374965dup GRCh37
NC_000019.8:g.56066777dup NCBI36
NG_031984.1:g.3277dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1474dup (KLK2) ENSP00000472852.1:n.-332-1474dup
ENST00000595375.5:n.149+960dup (KLK2)
ENST00000596950.5:n.113+852dup (KLK2)
ENST00000597509.5:n.243+852dup (KLK2)
XR_935817.1:n.1325-5972dup (KLK3)