Canonical Allele Identifier: CA633706699

Linked Data

dbSNP Id: rs1193837312

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871803T>C , CM000681.2:g.50871803T>C GRCh38
NC_000019.9:g.51375059T>C , CM000681.1:g.51375059T>C GRCh37
NC_000019.8:g.56066871T>C NCBI36
NG_031984.1:g.3371T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1380T>C (KLK2) ENSP00000472852.1:n.-332-1380T>C
ENST00000595375.5:n.149+1054T>C (KLK2)
ENST00000596950.5:n.113+946T>C (KLK2)
ENST00000597509.5:n.243+946T>C (KLK2)
XR_935817.1:n.1325-5878T>C (KLK3)