Canonical Allele Identifier: CA2662236445
Gene: FRZB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838678del , CM000664.2:g.182838678del GRCh38
NC_000002.11:g.183703406del , CM000664.1:g.183703406del GRCh37
NC_000002.10:g.183411651del NCBI36
NG_017197.1:g.33099del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-59del MANE Select ENSP00000295113.4:n.593-59del
ENST00000295113.4:c.593-59del ENSP00000295113.4:n.593-59del
NM_001463.3:c.593-59del NP_001454.2:n.593-59del
NM_001463.4:c.593-59del MANE Select NP_001454.2:n.593-59del