Canonical Allele Identifier: CA2662236437
Gene: FRZB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838664_182838671del , CM000664.2:g.182838664_182838671del GRCh38
NC_000002.11:g.183703392_183703399del , CM000664.1:g.183703392_183703399del GRCh37
NC_000002.10:g.183411637_183411644del NCBI36
NG_017197.1:g.33100_33107del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-58_593-51del MANE Select ENSP00000295113.4:n.593-58_593-51del
ENST00000295113.4:c.593-58_593-51del ENSP00000295113.4:n.593-58_593-51del
NM_001463.3:c.593-58_593-51del NP_001454.2:n.593-58_593-51del
NM_001463.4:c.593-58_593-51del MANE Select NP_001454.2:n.593-58_593-51del