Canonical Allele Identifier: CA2662236403
Gene: FRZB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838362del , CM000664.2:g.182838362del GRCh38
NC_000002.11:g.183703090del , CM000664.1:g.183703090del GRCh37
NC_000002.10:g.183411335del NCBI36
NG_017197.1:g.33409del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+47del MANE Select ENSP00000295113.4:n.797+47del
ENST00000295113.4:c.797+47del ENSP00000295113.4:n.797+47del
NM_001463.3:c.797+47del NP_001454.2:n.797+47del
NM_001463.4:c.797+47del MANE Select NP_001454.2:n.797+47del