Canonical Allele Identifier: CA14664379
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50870562A>G , CM000681.2:g.50870562A>G GRCh38
NC_000019.9:g.51373818A>G , CM000681.1:g.51373818A>G GRCh37
NC_000019.8:g.56065630A>G NCBI36
NG_031984.1:g.2130A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-2621A>G (KLK2) ENSP00000472852.1:n.-332-2621A>G
XR_935817.1:n.1325-7119A>G (KLK3)