Canonical Allele Identifier: CA2662236452

Gene: FRZB

Linked Data

• gnomAD v4: 2-182838681-CAAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182838682_182838685del , CM000664.2:g.182838682_182838685del	GRCh38
NC_000002.11:g.183703410_183703413del , CM000664.1:g.183703410_183703413del	GRCh37
NC_000002.10:g.183411655_183411658del	NCBI36
NG_017197.1:g.33086_33089del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295113.5:c.593-72_593-69del MANE Select	ENSP00000295113.4:n.593-72_593-69del
ENST00000295113.4:c.593-72_593-69del	ENSP00000295113.4:n.593-72_593-69del
NM_001463.3:c.593-72_593-69del	NP_001454.2:n.593-72_593-69del
NM_001463.4:c.593-72_593-69del MANE Select	NP_001454.2:n.593-72_593-69del