Canonical Allele Identifier: CA2565682837
Gene: FRZB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838230_182838231del , CM000664.2:g.182838230_182838231del GRCh38
NC_000002.11:g.183702958_183702959del , CM000664.1:g.183702958_183702959del GRCh37
NC_000002.10:g.183411203_183411204del NCBI36
NG_017197.1:g.33540_33541del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+178_797+179del MANE Select ENSP00000295113.4:n.797+178_797+179del
ENST00000295113.4:c.797+178_797+179del ENSP00000295113.4:n.797+178_797+179del
NM_001463.3:c.797+178_797+179del NP_001454.2:n.797+178_797+179del
NM_001463.4:c.797+178_797+179del MANE Select NP_001454.2:n.797+178_797+179del