Canonical Allele Identifier: CA1312516018
Gene: FRZB HGNC NCBI

Linked Data

dbSNP Id: rs1695556275

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838828dup , CM000664.2:g.182838828dup GRCh38
NC_000002.11:g.183703556dup , CM000664.1:g.183703556dup GRCh37
NC_000002.10:g.183411801dup NCBI36
NG_017197.1:g.32944dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.593-214dup MANE Select ENSP00000295113.4:n.593-214dup
ENST00000295113.4:c.593-214dup ENSP00000295113.4:n.593-214dup
NM_001463.3:c.593-214dup NP_001454.2:n.593-214dup
NM_001463.4:c.593-214dup MANE Select NP_001454.2:n.593-214dup