Canonical Allele Identifier: CA883226656

Genomic Alleles

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

Transcript Alleles

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