Canonical Allele Identifier: CA11117393
Gene: PLEK HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17035378

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68371823T>C , CM000664.2:g.68371823T>C GRCh38
NC_000002.10:g.68452459T>C NCBI36
NC_000002.11:g.68598955T>C , CM000664.1:g.68598955T>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000234313.7:c.42+6430T>C ENSP00000234313.7:p.=
NM_002664.2:c.42+6430T>C VV NP_002655.2:p.=
XM_011532916.1:c.42+6430T>C XP_011531218.1:p.=