Canonical Allele Identifier: CA2341121198

Linked Data

dbSNP Id: rs2090232200

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871694C>G , CM000681.2:g.50871694C>G GRCh38
NC_000019.9:g.51374950C>G , CM000681.1:g.51374950C>G GRCh37
NC_000019.8:g.56066762C>G NCBI36
NG_031984.1:g.3262C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1489C>G (KLK2) ENSP00000472852.1:n.-332-1489C>G
ENST00000595375.5:n.149+945C>G (KLK2)
ENST00000596950.5:n.113+837C>G (KLK2)
ENST00000597509.5:n.243+837C>G (KLK2)
XR_935817.1:n.1325-5987C>G (KLK3)