Canonical Allele Identifier: CA309642865

Linked Data

dbSNP Id: rs778877199

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871698C>G , CM000681.2:g.50871698C>G GRCh38
NC_000019.9:g.51374954C>G , CM000681.1:g.51374954C>G GRCh37
NC_000019.8:g.56066766C>G NCBI36
NG_031984.1:g.3266C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1485C>G (KLK2) ENSP00000472852.1:n.-332-1485C>G
ENST00000595375.5:n.149+949C>G (KLK2)
ENST00000596950.5:n.113+841C>G (KLK2)
ENST00000597509.5:n.243+841C>G (KLK2)
XR_935817.1:n.1325-5983C>G (KLK3)