Canonical Allele Identifier: CA2662236451
Gene: FRZB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838684del , CM000664.2:g.182838684del GRCh38
NC_000002.11:g.183703412del , CM000664.1:g.183703412del GRCh37
NC_000002.10:g.183411657del NCBI36
NG_017197.1:g.33089del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-69del MANE Select ENSP00000295113.4:n.593-69del
ENST00000295113.4:c.593-69del ENSP00000295113.4:n.593-69del
NM_001463.3:c.593-69del NP_001454.2:n.593-69del
NM_001463.4:c.593-69del MANE Select NP_001454.2:n.593-69del