Canonical Allele Identifier: CA2341121236

Linked Data

dbSNP Id: rs2090232942

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871774del , CM000681.2:g.50871774del GRCh38
NC_000019.9:g.51375030del , CM000681.1:g.51375030del GRCh37
NC_000019.8:g.56066842del NCBI36
NG_031984.1:g.3342del

Transcript Alleles

HGVS Amino-acid change
ENST00000593493.5:c.-332-1409del (KLK2) ENSP00000472852.1:n.-332-1409del
ENST00000595375.5:n.149+1025del (KLK2)
ENST00000596950.5:n.113+917del (KLK2)
ENST00000597509.5:n.243+917del (KLK2)
XR_935817.1:n.1325-5907del (KLK3)