Canonical Allele Identifier: CA1312515976
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695555402

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838726del , CM000664.2:g.182838726del GRCh38
NC_000002.11:g.183703454del , CM000664.1:g.183703454del GRCh37
NC_000002.10:g.183411699del NCBI36
NG_017197.1:g.33046del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-112del MANE Select ENSP00000295113.4:n.593-112del
ENST00000295113.4:c.593-112del ENSP00000295113.4:n.593-112del
NM_001463.3:c.593-112del NP_001454.2:n.593-112del
NM_001463.4:c.593-112del MANE Select NP_001454.2:n.593-112del