Canonical Allele Identifier: CA2814741001

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871679T>G , CM000681.2:g.50871679T>G GRCh38
NC_000019.9:g.51374935T>G , CM000681.1:g.51374935T>G GRCh37
NC_000019.8:g.56066747T>G NCBI36
NG_031984.1:g.3247T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1504T>G (KLK2) ENSP00000472852.1:n.-332-1504T>G
ENST00000595375.5:n.149+930T>G (KLK2)
ENST00000596950.5:n.113+822T>G (KLK2)
ENST00000597509.5:n.243+822T>G (KLK2)
XR_935817.1:n.1325-6002T>G (KLK3)