Canonical Allele Identifier: CA1312515962
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695555116

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838695del , CM000664.2:g.182838695del GRCh38
NC_000002.11:g.183703423del , CM000664.1:g.183703423del GRCh37
NC_000002.10:g.183411668del NCBI36
NG_017197.1:g.33076del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-82del MANE Select ENSP00000295113.4:n.593-82del
ENST00000295113.4:c.593-82del ENSP00000295113.4:n.593-82del
NM_001463.3:c.593-82del NP_001454.2:n.593-82del
NM_001463.4:c.593-82del MANE Select NP_001454.2:n.593-82del