Canonical Allele Identifier: CA2662236356
Gene: FRZB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838291dup , CM000664.2:g.182838291dup GRCh38
NC_000002.11:g.183703019dup , CM000664.1:g.183703019dup GRCh37
NC_000002.10:g.183411264dup NCBI36
NG_017197.1:g.33480dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.797+118dup MANE Select ENSP00000295113.4:n.797+118dup
ENST00000295113.4:c.797+118dup ENSP00000295113.4:n.797+118dup
NM_001463.3:c.797+118dup NP_001454.2:n.797+118dup
NM_001463.4:c.797+118dup MANE Select NP_001454.2:n.797+118dup