Canonical Allele Identifier: CA633706690

Linked Data

dbSNP Id: rs1568500651

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50871679del , CM000681.2:g.50871679del GRCh38
NC_000019.9:g.51374935del , CM000681.1:g.51374935del GRCh37
NC_000019.8:g.56066747del NCBI36
NG_031984.1:g.3247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593493.5:c.-332-1504del (KLK2) ENSP00000472852.1:n.-332-1504del
ENST00000595375.5:n.149+930del (KLK2)
ENST00000596950.5:n.113+822del (KLK2)
ENST00000597509.5:n.243+822del (KLK2)
XR_935817.1:n.1325-6002del (KLK3)