Canonical Allele Identifier: CA15957737
Gene: KLK2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs198978

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50879816G>T , CM000681.2:g.50879816G>T GRCh38
NC_000019.9:g.51383072G>T , CM000681.1:g.51383072G>T GRCh37
NC_000019.8:g.56074884G>T NCBI36
NG_031984.1:g.11384G>T

Transcript Alleles

HGVS Amino-acid change
NM_001002231.2:c.*1408G>T VV NP_001002231.1:p.=
NM_001256080.1:c.*1257G>T VV NP_001243009.1:p.=
NM_005551.4:c.*1257G>T VV NP_005542.1:p.=
NR_045762.1:n.2108G>T
NR_045763.1:n.2170G>T
NM_005551.5:c.*1257G>T VV MANE Preferred NP_005542.1:p.=
ENST00000325321.7:c.*1257G>T ENSP00000313581.2:p.=
ENST00000358049.8:c.*1408G>T ENSP00000350748.3:p.=
ENST00000391810.6:c.*1257G>T ENSP00000375686.2:p.=
ENST00000597439.1:c.*1572G>T ENSP00000471214.1:p.=