Canonical Allele Identifier: CA1312515995
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695555815
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838778_182838779del , CM000664.2:g.182838778_182838779del GRCh38
NC_000002.11:g.183703506_183703507del , CM000664.1:g.183703506_183703507del GRCh37
NC_000002.10:g.183411751_183411752del NCBI36
NG_017197.1:g.32997_32998del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-161_593-160del MANE Select ENSP00000295113.4:n.593-161_593-160del
ENST00000295113.4:c.593-161_593-160del ENSP00000295113.4:n.593-161_593-160del
NM_001463.3:c.593-161_593-160del NP_001454.2:n.593-161_593-160del
NM_001463.4:c.593-161_593-160del MANE Select NP_001454.2:n.593-161_593-160del
Search 100 bp 5'
Search 100 bp 3'