Canonical Allele Identifier: CA2662236421
Gene: FRZB HGNC NCBI

Linked Data

gnomAD v4: 2-182838577-C-CACTT
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.182838579_182838582dup , CM000664.2:g.182838579_182838582dup GRCh38
NC_000002.11:g.183703307_183703310dup , CM000664.1:g.183703307_183703310dup GRCh37
NC_000002.10:g.183411552_183411555dup NCBI36
NG_017197.1:g.33190_33193dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295113.5:c.625_628dup MANE Select ENSP00000295113.4:p.Cys210Ter
ENST00000295113.4:c.625_628dup ENSP00000295113.4:p.Cys210Ter
NM_001463.3:c.625_628dup NP_001454.2:p.Cys210Ter
NM_001463.4:c.625_628dup MANE Select NP_001454.2:p.Cys210Ter
Search 100 bp 5'
Search 100 bp 3'